Canonical Allele Identifier: PA2826636653
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619580
ClinVar RCV Id: RCV000758672 RCV002440585 RCV002533820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala613Thr
CA346755400
NM_001281494.2:c.1837G>A