Canonical Allele Identifier: PA2828394731
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 527264
ClinVar RCV Id: RCV000632115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357180.2:p.Tyr222Ser
CA381185215
NM_001370251.2:c.665A>C