Canonical Allele Identifier: PA2826625213
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234898
ClinVar RCV Id: RCV000220301 RCV001854763 RCV003998647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys187Arg
CA10577261
NM_001281492.2:c.560A>G