Canonical Allele Identifier: PA2573208317
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1590525
ClinVar RCV Id: RCV002103663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Ala130Thr
CA3565153
NM_001363626.2:c.388G>A