Allele Registry

Canonical Allele Identifier: PA2828400091

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000467767

ClinVar Variation:

403825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357190.2:p.Ser443Tyr	CA16613613 NM_001370261.2:c.1328C>A