Canonical Allele Identifier: PA2828401640
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16686
ClinVar RCV Id: RCV000018166 RCV000255755 RCV004018639
ClinVar Variation Id: 428003
ClinVar RCV Id: RCV000491105 RCV001390119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357191.2:p.Trp401Arg
CA009116
NM_001370262.2:c.1201T>A
CA223912292
NM_001370262.2:c.1201T>C