Allele Registry

Canonical Allele Identifier: PA2830171404

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000547991

RCV002377015

ClinVar Variation:

457284

HGVS (amino-acid)	Matching Registered Transcripts
NP_570711.2:p.Trp423Arg	CA381180422 NM_130799.3:c.1267T>A CA381180426 NM_130799.3:c.1267T>C