Canonical Allele Identifier: PA2830171812
Gene: MEN1 HGNC NCBI
ClinVar RCV:
RCV001342592
ClinVar Variation:
1039168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Thr568Ser
CA381177630
NM_130799.3:c.1703C>G
CA381177634
NM_130799.3:c.1702A>T