Canonical Allele Identifier: PA2741816722
Gene: XPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2531612
ClinVar RCV Id: RCV003249914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000371.1:p.Met263Ile
CA5148669
NM_000380.4:c.789G>A
CA374185320
NM_000380.4:c.789G>T
CA374185321
NM_000380.4:c.789G>C