ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658660508
Gene: FANCC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
456161
ClinVar RCV Id:
RCV000551381
RCV002323916
RCV003478126
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000127.2:p.Leu110Pro
CA5137779
NM_000136.3:c.329T>C