Canonical Allele Identifier: PA2741895827
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2631265
ClinVar RCV Id: RCV004531549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Lys217Arg
CA356138554
NM_002448.3:c.650A>G