Canonical Allele Identifier: PA2830176413
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1935496
ClinVar RCV Id: RCV002639023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570714.2:p.Thr443Ser
CA381180206
NM_130802.3:c.1328C>G
CA381180209
NM_130802.3:c.1327A>T