Canonical Allele Identifier: PA2826507018
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2696509
ClinVar RCV Id: RCV003539517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Gln61His
CA378382210
NM_001269039.3:c.183A>C
CA378382222
NM_001269039.3:c.183A>T