Canonical Allele Identifier: PA2741869492
Gene: MSX2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Pro131Leu
CA3565155
NM_001363626.2:c.392C>T