Canonical Allele Identifier: PA2830170901
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755784
ClinVar RCV Id: RCV002377987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Met228Ile
CA381184667
NM_130799.3:c.684G>T
CA381184668
NM_130799.3:c.684G>C
CA381184670
NM_130799.3:c.684G>A