Canonical Allele Identifier: PA658746790
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489985
ClinVar RCV Id: RCV000579759 RCV001371208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser860Cys
CA346754780
NM_000179.3:c.2579C>G