Canonical Allele Identifier: PA2830171391
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428083
ClinVar RCV Id: RCV000491697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Asp418Tyr
CA381180517
NM_130799.3:c.1252G>T
CA2695214593
NM_130799.3:c.1252_1254delinsTAT