Canonical Allele Identifier: PA2499261466
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299819
ClinVar RCV Id: RCV001730243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Arg202His
CA356138461
NM_002448.3:c.605G>A