Canonical Allele Identifier: PA2826628678
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823993
ClinVar RCV Id: RCV001020730 RCV001860995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1075Lys
CA346760576
NM_001281492.2:c.3224C>A