ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645455643
Gene: SHOC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000413825
RCV001584108
RCV002272224
RCV003539878
RCV003922677
ClinVar Variation:
373090
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031399.2:p.Met173Val
CA16042684
NM_007373.4:c.517A>G