Canonical Allele Identifier: PA2829764409
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 3065574
ClinVar RCV Id: RCV003990651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp2555Glu
CA387518517
NM_014363.6:c.7665T>G
CA387518518
NM_014363.6:c.7665T>A