Canonical Allele Identifier: PA2827689943
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1418862
ClinVar RCV Id: RCV001940533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339850.1:p.Ala46Thr
CA8818162
NM_001352921.3:c.136G>A