Canonical Allele Identifier: PA2828396929
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402532
ClinVar RCV Id: RCV001925152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357188.2:p.Glu486Asp
CA381179200
NM_001370259.2:c.1458G>C
CA381179206
NM_001370259.2:c.1458G>T