Canonical Allele Identifier: PA2826137906
Gene: ASNS HGNC NCBI

Linked Data

ClinVar Variation Id: 373307
ClinVar RCV Id: RCV000412830
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171548.1:p.Ser344Pro
CA16042617
NM_001178077.1:c.1030T>C