Canonical Allele Identifier: PA645378478
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410488
ClinVar RCV Id: RCV000468439 RCV001551754 RCV001023262 RCV004001843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His164Leu
CA073064
NM_000179.3:c.491A>T