Canonical Allele Identifier: PA2825100713
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403831
ClinVar RCV Id: RCV000470590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Ser258Trp
CA16613469
NM_000244.4:c.773C>G