Canonical Allele Identifier: PA2828776488
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711053
ClinVar RCV Id: RCV002292340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Val437Gly
CA369588924
NM_001378469.1:c.1310T>G