Canonical Allele Identifier: PA162918
Gene: XPC HGNC NCBI

Linked Data

ClinVar Variation Id: 135486
ClinVar RCV Id: RCV000122344 RCV000861309 RCV001150642 RCV002257449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004619.3:p.Arg594Cys
CA162916
NM_004628.4:c.1780C>T