Canonical Allele Identifier: PA2828100904
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 906444
ClinVar RCV Id: RCV001155621 RCV001155622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Lys105Asn
CA3565132
NM_001363626.2:c.315G>C
CA362229550
NM_001363626.2:c.315G>T