Canonical Allele Identifier: PA287189
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127532
ClinVar RCV Id: RCV000115342 RCV000709080 RCV003492471 RCV000805530 RCV001011247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg458Ser
CA287187
NM_000136.3:c.1374A>C
CA374106209
NM_000136.3:c.1374A>T