Canonical Allele Identifier: PA2573212170
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16695
ClinVar RCV Id: RCV000018175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357180.2:p.Glu401Lys
CA009018
NM_001370251.2:c.1200_1201delinsAA
CA223914042
NM_001370251.2:c.1201G>A