Canonical Allele Identifier: PA162932
Gene: XPC HGNC NCBI

Linked Data

ClinVar Variation Id: 135490
ClinVar RCV Id: RCV000122349 RCV000907099 RCV001150645 RCV003945106
ClinVar Variation Id: 343571
ClinVar RCV Id: RCV000669738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004619.3:p.Met513Ile
CA162930
NM_004628.4:c.1539G>C
CA2267415
NM_004628.4:c.1539G>A
CA351540156
NM_004628.4:c.1539G>T