Canonical Allele Identifier: PA2828400078
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357190.2:p.Trp436Cys
CA009127
NM_001370261.2:c.1308G>T
CA381180218
NM_001370261.2:c.1308G>C