Canonical Allele Identifier: PA2828100903
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2741449
ClinVar RCV Id: RCV003593507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Ala102Pro
CA362229527
NM_001363626.2:c.304G>C