Allele Registry

Canonical Allele Identifier: PA2828398807

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001342592

ClinVar Variation:

1039168

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357189.2:p.Thr568Ser	CA381177630 NM_001370260.2:c.1703C>G CA381177634 NM_001370260.2:c.1702A>T