Allele Registry

Canonical Allele Identifier: PA2825101522

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001928013

ClinVar Variation:

1410267

HGVS (amino-acid)	Matching Registered Transcripts
NP_000235.3:p.Thr557Ala	CA381177852 NM_000244.4:c.1669A>G