Canonical Allele Identifier: PA105659
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219192
ClinVar RCV Id: RCV000203576 RCV000690192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002440.2:p.Pro148Leu
CA251352
NM_002449.5:c.443C>T