Canonical Allele Identifier: PA2741869492
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2721852
ClinVar RCV Id: RCV003595331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Pro131Leu
CA3565155
NM_001363626.2:c.392C>T