Canonical Allele Identifier: PA2826627387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237158
ClinVar RCV Id: RCV000231716 RCV000483224 RCV000490886 RCV000986722 RCV003998718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn697Asp
CA10582063
NM_001281492.2:c.2089A>G