Canonical Allele Identifier: PA2826637492
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730311
ClinVar RCV Id: RCV002326487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn809_Ile813del
CA2580067063
NM_001281494.2:c.2424_2438del