Canonical Allele Identifier: PA658680948
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455190
ClinVar RCV Id: RCV000544057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu782Val
CA346753457
NM_000179.3:c.2344C>G