Canonical Allele Identifier: PA2828776990
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 55793
ClinVar RCV Id: RCV000049222 RCV000824914 RCV000788009 RCV001384671
ClinVar Variation Id: 180784
ClinVar RCV Id: RCV000157818 RCV000788010 RCV000824913 RCV000809145 RCV001803101 RCV001808428 RCV003992202
ClinVar Variation Id: 2674585
ClinVar RCV Id: RCV003454374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Phe213Leu
CA284654
NM_001378470.1:c.639T>G
CA295904
NM_001378470.1:c.637T>C
CA369590847
NM_001378470.1:c.639T>A