Allele Registry

Canonical Allele Identifier: PA2825100632

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000489379

RCV002367666

ClinVar Variation:

427122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000235.3:p.Trp225Arg	CA381185237 NM_000244.4:c.673T>A CA381185239 NM_000244.4:c.673T>C