Canonical Allele Identifier: PA2830171428
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16686
ClinVar Variation Id: 428003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Trp436Arg
CA009116
NM_130799.3:c.1306T>A
CA223912292
NM_130799.3:c.1306T>C