Canonical Allele Identifier: PA2828400074
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 836112
ClinVar RCV Id: RCV001037159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357190.2:p.His433Tyr
CA381180254
NM_001370261.2:c.1297C>T