Allele Registry

Canonical Allele Identifier: PA2830173470

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001342592

ClinVar Variation:

1039168

HGVS (amino-acid)	Matching Registered Transcripts
NP_570712.2:p.Thr573Ser	CA381177630 NM_130800.3:c.1718C>G CA381177634 NM_130800.3:c.1717A>T