Canonical Allele Identifier: PA2826592592
Gene: CST8 HGNC NCBI
ClinVar RCV:
RCV004271976
ClinVar Variation:
2481285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268659.1:p.Asn102Asp
CA408422295
NM_001281730.2:c.304A>G