Canonical Allele Identifier: PA916062037
Gene: CNNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 298634
ClinVar RCV Id: RCV000293358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_951059.1:p.Gln17Glu
CA10627963
NM_199077.3:c.49C>G