ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014834
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000548806
RCV000674060
ClinVar Variation:
456146
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.His322Tyr
CA8252610
NM_001286167.3:c.964C>T