Canonical Allele Identifier: PA645383089
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410482
ClinVar RCV Id: RCV002230416 RCV002436447 RCV004001842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg988Pro
CA069882
NM_000179.3:c.2963G>C