Canonical Allele Identifier: PA287215
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127541
ClinVar RCV Id: RCV000115352 RCV000315029 RCV000709093 RCV000571052 RCV001818267 RCV003492473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala132Gly
CA287213
NM_000136.3:c.395C>G