This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2580330934
Gene: CST8 HGNC NCBI
ClinVar RCV:
RCV004271976
ClinVar Variation:
2481285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005483.1:p.Asn102Asp
CA408422295
NM_005492.4:c.304A>G