Canonical Allele Identifier: PA2827628362
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321366
ClinVar RCV Id: RCV000274943 RCV001094307 RCV001820959 RCV003922359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Val198Ile
CA8252857
NM_001351830.2:c.592G>A