Canonical Allele Identifier: PA2826631655
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2134360
ClinVar RCV Id: RCV003044901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val506Ala
CA346754017
NM_001281493.2:c.1517T>C