Allele Registry

Canonical Allele Identifier: PA105555

Gene: MSX1 HGNC NCBI

ClinVar Allele:

227271

ClinVar RCV:

RCV000490415

RCV000950563

RCV004541305

ClinVar Variation:

225414

HGVS (amino-acid)	Matching Registered Transcripts
NP_002439.2:p.Arg157Ser	CA2833052 NM_002448.3:c.471G>T CA356138186 NM_002448.3:c.471G>C