Canonical Allele Identifier: PA2828082897
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1003782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350157.1:p.Leu535Pro
CA176076961
NM_001363228.2:c.1604T>C