Canonical Allele Identifier: PA2741945020
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2892958
ClinVar RCV Id: RCV003750599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Leu2076Val
CA6911115
NM_014363.6:c.6226T>G