Canonical Allele Identifier: PA2826636974
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233992
ClinVar RCV Id: RCV000222273 RCV000478635 RCV000464929 RCV003469091 RCV003998590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu690Lys
CA069899
NM_001281494.2:c.2068G>A