Canonical Allele Identifier: PA2826632820
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127583
ClinVar RCV Id: RCV000115408 RCV003593912 RCV002444567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile777Leu
CA012114
NM_001281493.2:c.2329A>C