Canonical Allele Identifier: PA916011029
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801218
ClinVar RCV Id: RCV000985825 RCV001052611 RCV001187791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly56Glu
CA346734985
NM_001281492.2:c.167G>A