Canonical Allele Identifier: PA2830170478
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Thr76Ser
CA381187607
NM_130799.3:c.227C>G
CA381187610
NM_130799.3:c.226A>T