Canonical Allele Identifier: PA645404662
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408204
ClinVar RCV Id: RCV000465004 RCV001508800 RCV003153618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala1284Pro
CA8250923
NM_000135.4:c.3850G>C