Canonical Allele Identifier: PA2826637570
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89378
ClinVar RCV Id: RCV000524174 RCV000573399 RCV001800369 RCV003460682 RCV003997088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr826Cys
CA012724
NM_001281494.2:c.2477A>G