Canonical Allele Identifier: PA2825101158
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428072
ClinVar Variation Id: 457285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Ser432Arg
CA381180329
NM_000244.4:c.1296T>G
CA381180331
NM_000244.4:c.1296T>A
CA381180344
NM_000244.4:c.1294A>C