Canonical Allele Identifier: PA2499252946
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1104168
ClinVar RCV Id: RCV001428105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Cys129Trp
CA362229708
NM_001363626.2:c.387C>G