Canonical Allele Identifier: PA287201
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu536Pro
CA287199
NM_000136.3:c.1607T>C