Canonical Allele Identifier: PA2828777222
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 177878
ClinVar RCV Id: RCV000154526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Lys449Asn
CA273507
NM_001378470.1:c.1347A>C
CA369588490
NM_001378470.1:c.1347A>T