Allele Registry

Canonical Allele Identifier: PA2573212649

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV001928013

ClinVar Variation:

1410267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357180.2:p.Thr594Ala	CA381177852 NM_001370251.2:c.1780A>G