Canonical Allele Identifier: PA2828100901
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 904830
ClinVar RCV Id: RCV001152974 RCV001152975 RCV001819860 RCV002032410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Val96Leu
CA3565124
NM_001363626.2:c.286G>T
CA362229490
NM_001363626.2:c.286G>C