Canonical Allele Identifier: PA2828402739
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403831
ClinVar RCV Id: RCV000470590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357192.2:p.Ser218Trp
CA16613469
NM_001370263.2:c.653C>G