ClinGen Allele Registry
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Canonical Allele Identifier:
PA645403725
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
326857
ClinVar RCV:
RCV000371929
RCV002522902
ClinVar Variation:
321370
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Ala129Val
CA8253042
NM_000135.4:c.386C>T