Canonical Allele Identifier: PA916035638
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 638088
ClinVar RCV Id: RCV000790554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339851.1:p.Arg150Trp
CA401362762
NM_001352922.2:c.448C>T