Canonical Allele Identifier: PA2828079823
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2354303
ClinVar RCV Id: RCV004192778
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350075.1:p.Leu271Met
CA187546895
NM_001363146.1:c.811C>A