Canonical Allele Identifier: PA2829385065
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3212900
ClinVar RCV Id: RCV004503820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Pro119Leu
CA3565143
NM_002449.5:c.356C>T