Canonical Allele Identifier: PA2825187725
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 1483851
ClinVar RCV Id: RCV001998985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Val126Leu
CA397087751
NM_000485.3:c.376G>T
CA397087754
NM_000485.3:c.376G>C