Allele Registry

Canonical Allele Identifier: PA2830173098

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000467767

ClinVar Variation:

403825

HGVS (amino-acid)	Matching Registered Transcripts
NP_570712.2:p.Ser448Tyr	CA16613613 NM_130800.3:c.1343C>A