Canonical Allele Identifier: PA2827690085
Gene: SGSH HGNC NCBI

Linked Data

ClinVar Variation Id: 552534
ClinVar RCV Id: RCV000667816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339850.1:p.Leu146Pro
CA8818015
NM_001352921.3:c.437T>C