Canonical Allele Identifier: PA645381918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419439
ClinVar RCV Id: RCV000483513 RCV003758786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu773Val
CA16617671
NM_000179.3:c.2317C>G