Allele Registry

Canonical Allele Identifier: PA2828403166

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000491697

ClinVar Variation:

428083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357192.2:p.Asp383Tyr	CA381180517 NM_001370263.2:c.1147G>T CA2695214593 NM_001370263.2:c.1147_1149delinsTAT