Canonical Allele Identifier: PA2828776481
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Pro431Leu
CA369588964
NM_001378469.1:c.1292C>T