Canonical Allele Identifier: PA2828100874
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389913
ClinVar RCV Id: RCV001898133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Pro28Leu
CA362229081
NM_001363626.2:c.83C>T