Canonical Allele Identifier: PA2827628261
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ser144Phe
CA8252945
NM_001351830.2:c.431C>T