Canonical Allele Identifier: PA2827628447
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237058
ClinVar RCV Id: RCV000231055 RCV001274646 RCV002261014 RCV004020741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ser258Tyr
CA8252715
NM_001351830.2:c.773C>A