Canonical Allele Identifier: PA2828396777
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16686
ClinVar Variation Id: 428003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357188.2:p.Trp436Arg
CA009116
NM_001370259.2:c.1306T>A
CA223912292
NM_001370259.2:c.1306T>C