Canonical Allele Identifier: PA2573075373
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_001365396.1:p.Phe250Leu
CA284654
NM_001378467.1:c.750T>G
CA295904
NM_001378467.1:c.748T>C
CA369590847
NM_001378467.1:c.750T>A