Canonical Allele Identifier: PA2826637759
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2572789
ClinVar RCV Id: RCV003314903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val930dup
CA2580612568
NM_001281494.2:c.2788_2790dup