Canonical Allele Identifier: PA1139701427
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 982731
ClinVar RCV Id: RCV001262377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Ala200Val
CA356138450
NM_002448.3:c.599C>T