Canonical Allele Identifier: PA2573223533
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503933
ClinVar RCV Id: RCV002047668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Pro284Ser
CA2833141
NM_002448.3:c.850C>T