Allele Registry

Canonical Allele Identifier: PA2825100538

Gene: MEN1 HGNC NCBI

ClinVar Allele:

31736

ClinVar RCV:

RCV000018177

ClinVar Variation:

16697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000235.3:p.Val189Glu	CA009488 NM_000244.4:c.566T>A