Canonical Allele Identifier: PA2827251459
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218698
ClinVar RCV Id: RCV000203043 RCV002272173 RCV002273987 RCV002515502 RCV003407717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Gln269Arg
CA249249
NM_001324337.2:c.806A>G