Canonical Allele Identifier: PA2827251404
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2957705
ClinVar RCV Id: RCV003811368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Arg190Lys
CA5689597
NM_001324337.2:c.569G>A