Canonical Allele Identifier: PA2828776598
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1380885
ClinVar RCV Id: RCV001895097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Phe526Leu
CA4516698
NM_001378469.1:c.1576T>C
CA369587959
NM_001378469.1:c.1578T>G
CA369587961
NM_001378469.1:c.1578T>A