Canonical Allele Identifier: PA2830178032
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428083
ClinVar RCV Id: RCV000491697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570715.2:p.Asp423Tyr
CA381180517
NM_130803.3:c.1267G>T
CA2695214593
NM_130803.3:c.1267_1269delinsTAT