Canonical Allele Identifier: PA645378506
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237210
ClinVar RCV Id: RCV000234715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro170Ser
CA10582040
NM_000179.3:c.508C>T