Canonical Allele Identifier: PA2828400062
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428072
ClinVar Variation Id: 457285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357190.2:p.Ser427Arg
CA381180329
NM_001370261.2:c.1281T>G
CA381180331
NM_001370261.2:c.1281T>A
CA381180344
NM_001370261.2:c.1279A>C