Allele Registry

Canonical Allele Identifier: PA105649

Gene: MSX2 HGNC NCBI

ClinVar RCV:

RCV000018474

RCV001210266

ClinVar Variation:

16961

HGVS (amino-acid)	Matching Registered Transcripts
NP_002440.2:p.Pro148His	CA341436 NM_002449.5:c.443C>A