Allele Registry

Canonical Allele Identifier: PA2830176373

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000491697

ClinVar Variation:

428083

HGVS (amino-acid)	Matching Registered Transcripts
NP_570714.2:p.Asp423Tyr	CA381180517 NM_130802.3:c.1267G>T CA2695214593 NM_130802.3:c.1267_1269delinsTAT