Allele Registry

Canonical Allele Identifier: PA2830178043

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000547991

RCV002377015

ClinVar Variation:

457284

HGVS (amino-acid)	Matching Registered Transcripts
NP_570715.2:p.Trp428Arg	CA381180422 NM_130803.3:c.1282T>A CA381180426 NM_130803.3:c.1282T>C