Canonical Allele Identifier: PA2827251277
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3161864
ClinVar RCV Id: RCV004451210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Lys7Asn
CA378380286
NM_001324337.2:c.21A>C
CA378380288
NM_001324337.2:c.21A>T