Canonical Allele Identifier: PA186021
Gene: CALM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001734.1:p.Asp96Val
CA186019
NM_001743.6:c.287A>T