Canonical Allele Identifier: PA645383356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237175
ClinVar RCV Id: RCV000227649 RCV000491202 RCV000985838 RCV002494619 RCV003998725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1024Trp
CA10582076
NM_000179.3:c.3070C>T