Canonical Allele Identifier: PA106535
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 638087
ClinVar RCV Id: RCV000790553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.Tyr40Asn
CA401364635
NM_000199.5:c.118T>A