Canonical Allele Identifier: PA110866
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237048
ClinVar RCV Id: RCV000230300 RCV000498721 RCV000665186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Thr1131Ala
CA8251197
NM_000135.4:c.3391A>G