Canonical Allele Identifier: PA2826586581
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099301
ClinVar RCV Id: RCV003021654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr982Ser
CA346761309
NM_001281494.2:c.2944A>T