Allele Registry

Canonical Allele Identifier: PA2825101489

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000121334

RCV000860147

RCV001425924

RCV002227065

ClinVar Variation:

134640

1102578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000235.3:p.Thr546Ala	CA060856 NM_000244.4:c.1636A>G CA2499221138 NM_000244.4:c.1635_1636delinsAG CA2499221139 NM_000244.4:c.1635_1636delinsTG