Canonical Allele Identifier: PA645404710
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 429862
ClinVar RCV Id: RCV000493395 RCV001834601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Thr1373Ala
CA8250780
NM_000135.4:c.4117A>G