Canonical Allele Identifier: PA2499235481
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 1026249
ClinVar RCV Id: RCV001326674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Val123Leu
CA8234435
NM_001030018.2:c.367G>C
CA397087825
NM_001030018.2:c.367G>T