Allele Registry

Canonical Allele Identifier: PA2828396473

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000494086

RCV001202722

ClinVar Variation:

429809

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357188.2:p.Asp315Tyr	CA061863 NM_001370259.2:c.943G>T