Canonical Allele Identifier: PA2828100869
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2168870
ClinVar RCV Id: RCV003100468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Glu15Lys
CA362229003
NM_001363626.2:c.43G>A