Canonical Allele Identifier: PA2826628071
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229716
ClinVar RCV Id: RCV000223636 RCV000465720 RCV000589846 RCV000708883 RCV003462404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg858Leu
CA069886
NM_001281492.2:c.2573G>T