Canonical Allele Identifier: PA2827628296
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321369
ClinVar RCV Id: RCV000280680 RCV000660417 RCV001753780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Leu161Val
CA8252926
NM_001351830.2:c.481C>G