Canonical Allele Identifier: PA2499298752
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1020636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689632.2:p.Val481Leu
CA4736879
NM_152419.3:c.1441G>T
CA371119942
NM_152419.3:c.1441G>C