Canonical Allele Identifier: PA2828082609
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 167177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350157.1:p.Pro237Gln
CA180114
NM_001363228.2:c.710C>A