Allele Registry

Canonical Allele Identifier: PA2828398741

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000793172

ClinVar Variation:

640201

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357189.2:p.Thr541Pro	CA381178066 NM_001370260.2:c.1621A>C