Allele Registry

Canonical Allele Identifier: PA2830172761

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000482667

RCV000491064

ClinVar Variation:

418293

HGVS (amino-acid)	Matching Registered Transcripts
NP_570712.2:p.Ser313Pro	CA16619359 NM_130800.3:c.937T>C