Canonical Allele Identifier: PA2826627168
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072092
ClinVar RCV Id: RCV004012122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys645Met
CA346753262
NM_001281492.2:c.1934A>T