Canonical Allele Identifier: PA2828400091
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403825
ClinVar RCV Id: RCV000467767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357190.2:p.Ser443Tyr
CA16613613
NM_001370261.2:c.1328C>A