Canonical Allele Identifier: PA2826632080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821707
ClinVar RCV Id: RCV001016390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr604Ile
CA346755352
NM_001281493.2:c.1811C>T