Canonical Allele Identifier: PA186031
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96722
ClinVar RCV Id: RCV000162069 RCV000143838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001734.1:p.Asp132Glu
CA186030
NM_001743.6:c.396T>G
CA346719047
NM_001743.6:c.396T>A