Canonical Allele Identifier: PA2580271830
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_002440.2:p.Glu15Lys
CA362229003
NM_002449.5:c.43G>A