ClinGen Allele Registry
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Canonical Allele Identifier:
PA645402493
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000221946
RCV000477104
RCV000575115
RCV001358152
RCV003144167
ClinVar Variation:
234311
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000127.2:p.Ala158Pro
CA10577378
NM_000136.3:c.472G>C