Allele Registry

Canonical Allele Identifier: PA2828399753

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000482667

RCV000491064

ClinVar Variation:

418293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357190.2:p.Ser308Pro	CA16619359 NM_001370261.2:c.922T>C