Canonical Allele Identifier: PA2828474171
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 55793
ClinVar Variation Id: 180784
ClinVar Variation Id: 2674585
ClinVar RCV Id: RCV003454374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Phe247Leu
CA284654
NM_001374244.1:c.741T>G
CA295904
NM_001374244.1:c.739T>C
CA369590847
NM_001374244.1:c.741T>A