ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA256209
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
27089
ClinVar RCV:
RCV000012830
ClinVar Variation:
12050
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000127.2:p.Leu496Arg
CA256207
NM_000136.3:c.1487T>G