Canonical Allele Identifier: PA2825084974
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3003810
ClinVar RCV Id: RCV003863385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu17Val
CA346734545
NM_000179.3:c.49C>G