Canonical Allele Identifier: PA2828779230
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44816
ClinVar Variation Id: 376289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Val548Leu
CA135104
NM_001378473.1:c.1642G>T
CA16602737
NM_001378473.1:c.1642G>C