Canonical Allele Identifier: PA2830171411
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428072
ClinVar Variation Id: 457285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Ser427Arg
CA381180329
NM_130799.3:c.1281T>G
CA381180331
NM_130799.3:c.1281T>A
CA381180344
NM_130799.3:c.1279A>C