Canonical Allele Identifier: PA2825187717
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 1026249
ClinVar RCV Id: RCV001326674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Val123Leu
CA8234435
NM_000485.3:c.367G>C
CA397087825
NM_000485.3:c.367G>T