Allele Registry

Canonical Allele Identifier: PA2573212666

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001342592

ClinVar Variation:

1039168

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357180.2:p.Thr610Ser	CA381177630 NM_001370251.2:c.1829C>G CA381177634 NM_001370251.2:c.1828A>T