Canonical Allele Identifier: PA195025
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89422
ClinVar RCV Id: RCV000166108 RCV000679239 RCV001302789 RCV003230394 RCV003450974 RCV003460687 RCV003997093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1193Lys
CA013478
NM_000179.3:c.3577G>A