Canonical Allele Identifier: PA2828398392
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_001357189.2:p.Asp418Tyr
CA381180517
NM_001370260.2:c.1252G>T
CA2695214593
NM_001370260.2:c.1252_1254delinsTAT