Canonical Allele Identifier: PA916026660
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 8525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309424.1:p.Arg164Gln
CA119690
NM_001322495.1:c.491G>A