Canonical Allele Identifier: PA2828776675
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44816
ClinVar RCV Id: RCV000037935 RCV000435048 RCV002463625
ClinVar Variation Id: 376289
ClinVar RCV Id: RCV000422356 RCV000856751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Val578Leu
CA135104
NM_001378469.1:c.1732G>T
CA16602737
NM_001378469.1:c.1732G>C