ClinGen Allele Registry
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Canonical Allele Identifier:
PA645403981
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000231055
RCV001274646
RCV002261014
RCV004020741
ClinVar Variation:
237058
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Ser290Tyr
CA8252715
NM_000135.4:c.869C>A