Canonical Allele Identifier: PA2573164436
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1403527
ClinVar RCV Id: RCV001909102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000190.1:p.His446Gln
CA8817604
NM_000199.5:c.1338C>G
CA401358649
NM_000199.5:c.1338C>A