Canonical Allele Identifier: PA2828100906
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2899561
ClinVar RCV Id: RCV003760312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Asp111Val
CA3565136
NM_001363626.2:c.332A>T