Canonical Allele Identifier: PA645378282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 423368
ClinVar RCV Id: RCV000482176 RCV000557696 RCV000560960 RCV004003399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro59Ser
CA068115
NM_000179.3:c.175C>T