ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826507232
Gene: SHOC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1403719
ClinVar RCV Id:
RCV001909194
RCV002359394
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001255968.1:p.Thr206Ala
CA5689603
NM_001269039.3:c.616A>G