Canonical Allele Identifier: PA2741895843
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2898205
ClinVar RCV Id: RCV003760295
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Ser43Pro
CA362229172
NM_002449.5:c.127T>C