Allele Registry

Canonical Allele Identifier: PA2830170757

Gene: MEN1 HGNC NCBI

ClinVar Allele:

171149

ClinVar RCV:

RCV000148612

RCV000410523

RCV000455664

RCV000569499

RCV000766972

RCV003153432

ClinVar Variation:

161294

HGVS (amino-acid)	Matching Registered Transcripts
NP_570711.2:p.Arg171Trp	CA009448 NM_130799.3:c.511C>T