Canonical Allele Identifier: PA339014
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216285
ClinVar RCV Id: RCV000199976 RCV000520121 RCV001167954 RCV001012322 RCV003153471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg532Lys
CA339012
NM_000136.3:c.1595G>A