Canonical Allele Identifier: PA2573274725
Gene: CNNM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484748
ClinVar RCV Id: RCV002006030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064569.3:p.Ser142Arg
CA347713689
NM_020184.4:c.424A>C
CA347713713
NM_020184.4:c.426C>A
CA347713716
NM_020184.4:c.426C>G