Canonical Allele Identifier: PA2828775182
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1351912
ClinVar RCV Id: RCV002049339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Met487Ile
CA4516724
NM_001378467.1:c.1461G>A
CA369588482
NM_001378467.1:c.1461G>C
CA369588483
NM_001378467.1:c.1461G>T