ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2827251296
Gene: SHOC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1760674
ClinVar RCV Id:
RCV002409893
RCV003099751
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001311266.1:p.Lys26Arg
CA5689550
NM_001324337.2:c.77A>G