Canonical Allele Identifier: PA1139690991
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 969540
ClinVar RCV Id: RCV001244915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys931Thr
CA071876
NM_001281494.2:c.2792A>C