Canonical Allele Identifier: PA2828398629
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403821
ClinVar RCV Id: RCV000458972 RCV000566191 RCV003392264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357189.2:p.Lys502Asn
CA060705
NM_001370260.2:c.1506G>C
CA381178780
NM_001370260.2:c.1506G>T