Canonical Allele Identifier: PA2830171029
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428031
ClinVar RCV Id: RCV000490992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Gly281Arg
CA381183705
NM_130799.3:c.841G>A
CA381183707
NM_130799.3:c.841G>C