Canonical Allele Identifier: PA2828400589
Gene: MEN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357191.2:p.Pro12Leu
CA009390
NM_001370262.2:c.35C>T