Canonical Allele Identifier: PA2830170771
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 656639
ClinVar RCV Id: RCV000813107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Leu177Val
CA381185929
NM_130799.3:c.529C>G