Canonical Allele Identifier: PA2826636435
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410399
ClinVar RCV Id: RCV000771517 RCV000464988 RCV001798840 RCV002289613 RCV004000830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met566Thr
CA069266
NM_001281494.2:c.1697T>C