Canonical Allele Identifier: PA645390441
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 427177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689632.2:p.Thr545Lys
CA4736988
NM_152419.3:c.1634C>A