Allele Registry

Canonical Allele Identifier: PA3057535764

Gene: MSX2 HGNC NCBI

ClinVar RCV:

RCV005183215

ClinVar Variation:

3701851

HGVS (amino-acid)	Matching Registered Transcripts
NP_002440.2:p.Met129Arg	CA3565195 NM_002449.5:c.386T>G