Canonical Allele Identifier: PA658808705
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 496951
ClinVar RCV Id: RCV000593641 RCV003465330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro4539Ser
CA387504864
NM_014363.6:c.13615C>T