Canonical Allele Identifier: PA2830170965
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403831
ClinVar RCV Id: RCV000470590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Ser253Trp
CA16613469
NM_130799.3:c.758C>G