Canonical Allele Identifier: PA2828100867
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468499
ClinVar RCV Id: RCV001993685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Asn8His
CA362228953
NM_001363626.2:c.22A>C