Canonical Allele Identifier: PA915992373
Gene: MSX2 HGNC NCBI
ClinVar RCV:
RCV000792855
ClinVar Variation:
639933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Pro148Ser
CA362229886
NM_002449.5:c.442C>T