Canonical Allele Identifier: PA916020311
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292555.1:p.Asp96Glu
CA186030
NM_001305626.1:c.288T>G
CA346719047
NM_001305626.1:c.288T>A