Canonical Allele Identifier: PA2826625120
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 663870
ClinVar RCV Id: RCV000821839 RCV002372347 RCV003461275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val166Gly
CA346740681
NM_001281492.2:c.497T>G