Canonical Allele Identifier: PA915992373
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639933
ClinVar RCV Id: RCV000792855
JSON-LD

Amino-acid Alleles

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