Canonical Allele Identifier: PA916014963
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408167
ClinVar RCV Id: RCV000458018 RCV001274572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gly811Asp
CA8251729
NM_001286167.3:c.2432G>A