Allele Registry

Canonical Allele Identifier: PA2580135859

Gene: MESP2 HGNC NCBI

ClinVar RCV:

RCV002922502

ClinVar Variation:

2053439

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035047.1:p.Glu103Lys	CA7730390 NM_001039958.2:c.307G>A