Canonical Allele Identifier: PA357400
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219868
ClinVar RCV Id: RCV000204386 RCV000482986 RCV000575872 RCV000986699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro85Ser
CA069156
NM_000179.3:c.253C>T