Canonical Allele Identifier: PA2825101569
Gene: MEN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000235.3:p.Ala579Thr
CA381177582
NM_000244.4:c.1735G>A