Canonical Allele Identifier: PA1139735161
Gene: CNNM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 895045
ClinVar RCV Id: RCV001136913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064569.3:p.Ala149Ser
CA347713830
NM_020184.4:c.445G>T