Allele Registry

Canonical Allele Identifier: PA343157

Gene: MESP2 HGNC NCBI

ClinVar RCV:

RCV000032156

ClinVar Variation:

38908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035047.1:p.Lys91Glu	CA343156 NM_001039958.2:c.271A>G