Canonical Allele Identifier: PA1139736663
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 958222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339851.1:p.Gln147Arg
CA401362804
NM_001352922.2:c.440A>G