Canonical Allele Identifier: PA658661153
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala624Gly
CA8251997
NM_000135.4:c.1871C>G