Allele Registry

Canonical Allele Identifier: PA343159

Gene: MESP2 HGNC NCBI

ClinVar RCV:

RCV000032157

ClinVar Variation:

38909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035047.1:p.Ile129Phe	CA343158 NM_001039958.2:c.385A>T