Canonical Allele Identifier: PA645404672
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321329
ClinVar RCV Id: RCV000368836 RCV001094402 RCV001820952 RCV003477891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1317Gln
CA8250852
NM_000135.4:c.3950G>A