Canonical Allele Identifier: PA2826633581
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479705
ClinVar RCV Id: RCV001991014 RCV003170336 RCV003464348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr941Pro
CA346761029
NM_001281493.2:c.2821A>C