Allele Registry

Canonical Allele Identifier: PA2828402874

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000482667

RCV000491064

ClinVar Variation:

418293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357192.2:p.Ser273Pro	CA16619359 NM_001370263.2:c.817T>C