Canonical Allele Identifier: PA915992357
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 703322
ClinVar RCV Id: RCV001503619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Pro260Thr
CA2833115
NM_002448.3:c.778C>A