Canonical Allele Identifier: PA162834
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 135458
ClinVar RCV Id: RCV000122316 RCV000665704 RCV000930543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Leu191Val
CA162832
NM_000380.4:c.571C>G