Canonical Allele Identifier: PA2830175096
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16698
ClinVar RCV Id: RCV000018178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570713.2:p.Thr557Ser
CA009261
NM_130801.3:c.1669A>T
CA381177843
NM_130801.3:c.1670C>G