Canonical Allele Identifier: PA2827883440
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1380885
ClinVar RCV Id: RCV001895097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Phe548Leu
CA4516698
NM_001354609.2:c.1642T>C
CA369587959
NM_001354609.2:c.1644T>G
CA369587961
NM_001354609.2:c.1644T>A