Canonical Allele Identifier: PA2828775175
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1315931
ClinVar RCV Id: RCV001757378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Val485Leu
CA369588499
NM_001378467.1:c.1453G>T
CA369588500
NM_001378467.1:c.1453G>C