Canonical Allele Identifier: PA2573274735
Gene: CNNM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1382593
ClinVar RCV Id: RCV001890406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064569.3:p.Asp165Ala
CA347714060
NM_020184.4:c.494A>C