Allele Registry

Canonical Allele Identifier: PA124427

Gene: MSX1 HGNC NCBI

ClinVar RCV:

RCV000016010

RCV001374733

ClinVar Variation:

14881

1064708

HGVS (amino-acid)	Matching Registered Transcripts
NP_002439.2:p.Gln193Ter