Allele Registry

Canonical Allele Identifier: PA2573208316

Gene: MSX2 HGNC NCBI

ClinVar RCV:

RCV002079845

RCV002512171

ClinVar Variation:

1528926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350555.1:p.Cys129Ser	CA3565152 NM_001363626.2:c.386G>C CA362229704 NM_001363626.2:c.385T>A