Canonical Allele Identifier: PA2826634156
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 570267
ClinVar RCV Id: RCV000691090 RCV002325380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His1049Tyr
CA346761717
NM_001281493.2:c.3145C>T