Allele Registry

Canonical Allele Identifier: PA2828401640

Gene: MEN1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

31725

419793

ClinVar RCV:

RCV000018166

RCV000255755

RCV000491105

RCV001390119

RCV004018639

ClinVar Variation:

16686

428003

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357191.2:p.Trp401Arg	CA009116 NM_001370262.2:c.1201T>A CA223912292 NM_001370262.2:c.1201T>C