Canonical Allele Identifier: PA2830170885
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 427122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Trp220Arg
CA381185237
NM_130799.3:c.658T>A
CA381185239
NM_130799.3:c.658T>C