Canonical Allele Identifier: PA2830176802
Gene: MEN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570714.2:p.Ala579Thr
CA381177582
NM_130802.3:c.1735G>A