Canonical Allele Identifier: PA2580271832
Gene: MSX2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Gly17Val
CA362229022
NM_002449.5:c.50G>T