ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827251272
Gene: SHOC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2265459
ClinVar RCV Id:
RCV004120669
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001311266.1:p.Ser2Thr
CA378380117
NM_001324337.2:c.5G>C