Canonical Allele Identifier: PA891846263
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568239
ClinVar RCV Id: RCV000688534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser998Pro
CA346756382
NM_000179.3:c.2992T>C