Canonical Allele Identifier: PA2828779953
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44816
ClinVar Variation Id: 376289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Val600Leu
CA135104
NM_001378474.1:c.1798G>T
CA16602737
NM_001378474.1:c.1798G>C