Canonical Allele Identifier: PA2580271810
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420915
ClinVar RCV Id: RCV003122080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Ala182Val
CA2833071
NM_002448.3:c.545C>T