ClinGen Allele Registry
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Canonical Allele Identifier:
PA356218
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
221841
ClinVar RCV:
RCV000206395
RCV000479585
RCV002426960
ClinVar Variation:
219624
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000127.2:p.Arg361Trp
CA350435
NM_000136.3:c.1081C>T