Canonical Allele Identifier: PA2826630421
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 926655
ClinVar RCV Id: RCV001189349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser223Thr
CA346746817
NM_001281493.2:c.668G>C