Canonical Allele Identifier: PA113684
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 18296
ClinVar RCV Id: RCV000019958 RCV000033908
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Met136Thr
CA128035
NM_000485.3:c.407T>C