Canonical Allele Identifier: PA2573274732
Gene: CNNM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419642
ClinVar RCV Id: RCV001910511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064569.3:p.Gly158Arg
CA1783216
NM_020184.4:c.472G>C
CA347713955
NM_020184.4:c.472G>A