Canonical Allele Identifier: PA2826632619
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216311
ClinVar RCV Id: RCV000196222 RCV000568269 RCV000759859 RCV002272172 RCV003320595 RCV003997000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg733Gln
CA070064
NM_001281493.2:c.2198G>A