Canonical Allele Identifier: PA186035
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001734.1:p.Gln136Pro
CA186033
NM_001743.6:c.407A>C