Canonical Allele Identifier: PA2826634254
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110673
ClinVar RCV Id: RCV003020300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg14Met
CA346740805
NM_001281494.2:c.41G>T