Canonical Allele Identifier: PA2828100881
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376736
ClinVar RCV Id: RCV001912092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Ser48Thr
CA362229206
NM_001363626.2:c.143G>C