Canonical Allele Identifier: PA2826631111
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 576711
ClinVar RCV Id: RCV000699274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu377Val
CA346750732
NM_001281493.2:c.1129T>G