Canonical Allele Identifier: PA2828397800
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 136170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357189.2:p.Asn189Ser
CA009502
NM_001370260.2:c.566A>G