Canonical Allele Identifier: PA166800
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141924
ClinVar RCV Id: RCV000130636 RCV000556805 RCV001030499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1230Gly
CA013825
NM_000179.3:c.3689C>G