Canonical Allele Identifier: PA106287
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 5117
ClinVar RCV Id: RCV000005424 RCV000078349 RCV003894791
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.Glu369Lys
CA117264
NM_000199.5:c.1105G>A