Allele Registry

Canonical Allele Identifier: PA2828403547

Gene: MEN1 HGNC NCBI

ClinVar RCV:

RCV000018178

ClinVar Variation:

16698

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357192.2:p.Thr517Ser	CA009261 NM_001370263.2:c.1549A>T CA381177843 NM_001370263.2:c.1550C>G