Allele Registry

Canonical Allele Identifier: PA2828397790

Gene: MEN1 HGNC NCBI

ClinVar Allele:

31736

ClinVar RCV:

RCV000018177

ClinVar Variation:

16697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357189.2:p.Val184Glu	CA009488 NM_001370260.2:c.551T>A