Canonical Allele Identifier: PA2827250978
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014118
ClinVar RCV Id: RCV001312811 RCV003135959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ala78Val
CA5689564
NM_001324336.2:c.233C>T