ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826331392
Gene: FANCC
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000709084
RCV001017185
RCV001825407
RCV003492140
ClinVar Variation:
584738
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001230672.1:p.Gln357Glu
CA5137482
NM_001243743.2:c.1069C>G