Canonical Allele Identifier: PA2828398722
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365107
ClinVar RCV Id: RCV001907841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357189.2:p.Thr534Met
CA381178184
NM_001370260.2:c.1601C>T