Canonical Allele Identifier: PA2827250979
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2725429
ClinVar RCV Id: RCV003540051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Pro79Arg
CA378382866
NM_001324336.2:c.236C>G