Canonical Allele Identifier: PA2828396788
Gene: MEN1 HGNC NCBI
ClinVar RCV:
RCV000467767
ClinVar Variation:
403825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357188.2:p.Ser443Tyr
CA16613613
NM_001370259.2:c.1328C>A