Canonical Allele Identifier: PA186029
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96721
ClinVar RCV Id: RCV000143837 RCV000162068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001734.1:p.Asn98Ile
CA186027
NM_001743.6:c.293A>T