Canonical Allele Identifier: PA2830179405
Gene: MEN1 HGNC NCBI
ClinVar RCV:
RCV001342592
ClinVar Variation:
1039168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570716.2:p.Thr573Ser
CA381177630
NM_130804.3:c.1718C>G
CA381177634
NM_130804.3:c.1717A>T