Canonical Allele Identifier: PA2825100666
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 655795
ClinVar RCV Id: RCV000812047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Lys238Thr
CA381184612
NM_000244.4:c.713A>C