Allele Registry

Canonical Allele Identifier: PA2828401752

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001237059

ClinVar Variation:

963085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357191.2:p.Trp436Ser	CA381179523 NM_001370262.2:c.1307G>C