Canonical Allele Identifier: PA2825055957
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 855889
ClinVar RCV Id: RCV001061237 RCV002339300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile398Met
CA5137422
NM_000136.3:c.1194T>G