Canonical Allele Identifier: PA1139701489
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 904829
ClinVar RCV Id: RCV001152973 RCV001152972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Lys41Met
CA362229161
NM_002449.5:c.122A>T