Canonical Allele Identifier: PA2826637643
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720068
ClinVar RCV Id: RCV002305085 RCV003308118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro867Arg
CA346760181
NM_001281494.2:c.2600C>G