ClinGen Allele Registry
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Canonical Allele Identifier:
PA658800273
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
526419
ClinVar RCV Id:
RCV000630946
RCV002261136
RCV002528848
RCV001274554
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Ala1284Thr
CA8250924
NM_000135.4:c.3850G>A