Allele Registry

Canonical Allele Identifier: PA3057505581

Gene: MESP2 HGNC NCBI

ClinVar RCV:

RCV005078289

ClinVar Variation:

3626639

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035047.1:p.Gly81Arg	CA274596800 NM_001039958.2:c.241G>C CA393769372 NM_001039958.2:c.241G>A