Canonical Allele Identifier: PA2826634281
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 942199
ClinVar RCV Id: RCV001212137 RCV001800969 RCV002375168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser19Leu
CA346740912
NM_001281494.2:c.56C>T