Canonical Allele Identifier: PA1139731518
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 990737
ClinVar RCV Id: RCV001278822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Val2923Ala
CA387515903
NM_014363.6:c.8768T>C