Canonical Allele Identifier: PA2828779760
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Pro453Leu
CA369588964
NM_001378474.1:c.1358C>T