Canonical Allele Identifier: PA2826631629
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842796
ClinVar RCV Id: RCV001045275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro500Thr
CA346753937
NM_001281493.2:c.1498C>A