Canonical Allele Identifier: PA916031228
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 649143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ala118Val
CA397480988
NM_001351830.2:c.353C>T