Canonical Allele Identifier: PA2827883317
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Pro453Leu
CA369588964
NM_001354609.2:c.1358C>T