Allele Registry

Canonical Allele Identifier: PA2828399534

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000489379

RCV002367666

ClinVar Variation:

427122

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357190.2:p.Trp220Arg	CA381185237 NM_001370261.2:c.658T>A CA381185239 NM_001370261.2:c.658T>C