Canonical Allele Identifier: PA2830170682
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Ser145Arg
CA381186694
NM_130799.3:c.435C>G
CA381186696
NM_130799.3:c.435C>A
CA381186707
NM_130799.3:c.433A>C