Canonical Allele Identifier: PA2825187719
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2115627
ClinVar RCV Id: RCV003046556
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Val126del
CA2580613920
NM_000485.3:c.375_377del