Canonical Allele Identifier: PA2499285748
Gene: CNNM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018198
ClinVar RCV Id: RCV001317464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064569.3:p.Glu143Asp
CA1783208
NM_020184.4:c.429G>C
CA347713733
NM_020184.4:c.429G>T