Canonical Allele Identifier: PA1139701423
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 947690
ClinVar RCV Id: RCV001218812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Lys194Arg
CA2833078
NM_002448.3:c.581A>G