Canonical Allele Identifier: PA2825051726
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1369364
ClinVar RCV Id: RCV001870590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Cys125Ser
CA397480951
NM_000135.4:c.374G>C
CA397480953
NM_000135.4:c.373T>A