Canonical Allele Identifier: PA2741895850
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2741449
ClinVar RCV Id: RCV003593507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Ala102Pro
CA362229527
NM_002449.5:c.304G>C