Canonical Allele Identifier: PA186028
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_001292554.1:p.Asn62Ile
CA186027
NM_001305625.2:c.185A>T