Canonical Allele Identifier: PA2826634340
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 632906
ClinVar RCV Id: RCV000780473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys32Thr
CA346741177
NM_001281494.2:c.95A>C