Canonical Allele Identifier: PA2828777899
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13975
ClinVar Variation Id: 177844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Leu448Phe
CA273414
NM_001378471.1:c.1344G>C
CA280060
NM_001378471.1:c.1344G>T