Canonical Allele Identifier: PA2573223539
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357486
ClinVar RCV Id: RCV001863829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Pro26Leu
CA3565099
NM_002449.5:c.77C>T