Canonical Allele Identifier: PA915964738
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820521
ClinVar RCV Id: RCV001014059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser668Tyr
CA346750670
NM_000179.3:c.2003C>A