Allele Registry

Canonical Allele Identifier: PA105629

Gene: MSX2 HGNC NCBI

ClinVar RCV:

RCV000018476

ClinVar Variation:

16963

HGVS (amino-acid)	Matching Registered Transcripts
NP_002440.2:p.Arg172His	CA127003 NM_002449.5:c.515G>A