Canonical Allele Identifier: PA645404265
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 425115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg880Gly
CA16621696
NM_000135.4:c.2638C>G