Canonical Allele Identifier: PA2830171859
Gene: MEN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Thr594Pro
CA381177324
NM_130799.3:c.1780A>C