Canonical Allele Identifier: PA2825187756
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988025
ClinVar RCV Id: RCV001269417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Ter181Arg
CA8234339
NM_000485.3:c.541T>C
CA397086032
NM_000485.3:c.541T>A