ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645455641
Gene: SHOC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
372586
ClinVar RCV Id:
RCV000412927
RCV002481272
RCV002524636
RCV004022163
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031399.2:p.Arg172Trp
CA16042705
NM_007373.4:c.514C>T