Canonical Allele Identifier: PA1139701504
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 904831
ClinVar RCV Id: RCV001152976 RCV001152977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Ala102Thr
CA3565130
NM_002449.5:c.304G>A