Canonical Allele Identifier: PA2580233069
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Pro493Leu
CA369588964
NM_001374258.1:c.1478C>T