Canonical Allele Identifier: PA2580271802
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1971993
ClinVar RCV Id: RCV002745849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Arg176Gln
CA356138299
NM_002448.3:c.527G>A