Canonical Allele Identifier: PA1139743297
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44816
ClinVar Variation Id: 376289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Val640Leu
CA135104
NM_001374258.1:c.1918G>T
CA16602737
NM_001374258.1:c.1918G>C