Canonical Allele Identifier: PA2825101173
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16686
ClinVar Variation Id: 428003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Trp441Arg
CA009116
NM_000244.4:c.1321T>A
CA223912292
NM_000244.4:c.1321T>C