ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827250950
Gene: SHOC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1514651
ClinVar RCV Id:
RCV002048309
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001311265.1:p.Gly35Trp
CA378381372
NM_001324336.2:c.103G>T