Canonical Allele Identifier: PA2830176610
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570714.2:p.Lys507Asn
CA060705
NM_130802.3:c.1521G>C
CA381178780
NM_130802.3:c.1521G>T