Canonical Allele Identifier: PA162935
Gene: XPC HGNC NCBI

Linked Data

ClinVar Variation Id: 135491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004619.3:p.Phe614Ser
CA162933
NM_004628.4:c.1841T>C