Canonical Allele Identifier: PA658826904
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 559102
ClinVar RCV Id: RCV000676147 RCV001063475 RCV002532173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.Ala434Val
CA8817621
NM_000199.5:c.1301C>T