Canonical Allele Identifier: PA2827628277
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Leu153Ile
CA159364
NM_001351830.2:c.457C>A