Canonical Allele Identifier: PA658815541
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536455
ClinVar RCV Id: RCV000644909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Ala233Val
CA3565247
NM_002449.5:c.698C>T