Allele Registry

Canonical Allele Identifier: PA2828400392

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000121334

RCV000860147

RCV001425924

RCV002227065

ClinVar Variation:

134640

1102578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357190.2:p.Thr541Ala	CA060856 NM_001370261.2:c.1621A>G CA2499221138 NM_001370261.2:c.1620_1621delinsAG CA2499221139 NM_001370261.2:c.1620_1621delinsTG