Canonical Allele Identifier: PA2828779767
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711053
ClinVar RCV Id: RCV002292340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Val459Gly
CA369588924
NM_001378474.1:c.1376T>G