Canonical Allele Identifier: PA2573223511
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418913
ClinVar RCV Id: RCV001954469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Ala182Thr
CA2833070
NM_002448.3:c.544G>A