ClinGen Allele Registry
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Canonical Allele Identifier:
PA645403564
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
336758
ClinVar RCV:
RCV000306986
RCV003477894
ClinVar Variation:
321375
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Arg20Lys
CA8253263
NM_000135.4:c.59G>A