Canonical Allele Identifier: PA2828777729
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1188158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Pro301Ser
CA4516878
NM_001378471.1:c.901C>T