Canonical Allele Identifier: PA2827883507
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44816
ClinVar Variation Id: 376289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Val600Leu
CA135104
NM_001354609.2:c.1798G>T
CA16602737
NM_001354609.2:c.1798G>C