Canonical Allele Identifier: PA2826637391
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89359
ClinVar RCV Id: RCV000131160 RCV000212679 RCV001137558 RCV001083021 RCV003153343 RCV004537277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785Thr
CA012215
NM_001281494.2:c.2353C>A