Canonical Allele Identifier: PA2826628680
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076149
ClinVar RCV Id: RCV004018466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1076Thr
CA346760578
NM_001281492.2:c.3226G>A