Canonical Allele Identifier: PA2826630422
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230508
ClinVar RCV Id: RCV004520659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser223Ile
CA346746814
NM_001281493.2:c.668G>T