Allele Registry

Canonical Allele Identifier: PA2828396028

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000491902

RCV001000177

ClinVar Variation:

428091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357188.2:p.Phe144Val	CA381186717 NM_001370259.2:c.430T>G