Allele Registry

Canonical Allele Identifier: PA2828396887

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001237059

ClinVar Variation:

963085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357188.2:p.Trp471Ser	CA381179523 NM_001370259.2:c.1412G>C