Canonical Allele Identifier: PA915964427
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 658746
ClinVar RCV Id: RCV000815628 RCV002406854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr605Asn
CA346749408
NM_000179.3:c.1814C>A