Canonical Allele Identifier: PA2828398439
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403825
ClinVar RCV Id: RCV000467767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357189.2:p.Ser443Tyr
CA16613613
NM_001370260.2:c.1328C>A