Canonical Allele Identifier: PA110632
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408175
ClinVar RCV Id: RCV000459562 RCV000779200 RCV001557545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1400His
CA8250692
NM_000135.4:c.4199G>A