Canonical Allele Identifier: PA2580271828
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2026310
ClinVar RCV Id: RCV002871293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Asn8Ser
CA3565090
NM_002449.5:c.23A>G