Canonical Allele Identifier: PA2828100865
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2907304
ClinVar RCV Id: RCV003760429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Met1Thr