Canonical Allele Identifier: PA2828776547
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13975
ClinVar Variation Id: 177844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Leu463Phe
CA273414
NM_001378469.1:c.1389G>C
CA280060
NM_001378469.1:c.1389G>T