Canonical Allele Identifier: PA2741895854
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2726611
ClinVar RCV Id: RCV003595440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Ala113Val
CA3565138
NM_002449.5:c.338C>T