Canonical Allele Identifier: PA186032
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96722
ClinVar RCV Id: RCV000162069 RCV000143838
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292554.1:p.Asp96Glu
CA186030
NM_001305625.2:c.288T>G
CA346719047
NM_001305625.2:c.288T>A