Canonical Allele Identifier: PA916031198
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237054
ClinVar RCV Id: RCV000233505 RCV000665027 RCV001770188 RCV001818561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Asp14Gly
CA8253266
NM_001351830.2:c.41A>G