Canonical Allele Identifier: PA2826586541
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735481
ClinVar RCV Id: RCV002364100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile981Asn
CA346761304
NM_001281494.2:c.2942T>A