Canonical Allele Identifier: PA2825101138
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428083
ClinVar RCV Id: RCV000491697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Asp423Tyr
CA381180517
NM_000244.4:c.1267G>T
CA2695214593
NM_000244.4:c.1267_1269delinsTAT