Canonical Allele Identifier: PA2826633282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89409
ClinVar RCV Id: RCV000486053 RCV000556518 RCV000565574 RCV000662821 RCV002267830 RCV003997092
ClinVar Variation Id: 578919
ClinVar RCV Id: RCV000702066 RCV004026579 RCV003999723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp879Glu
CA013331
NM_001281493.2:c.2637C>G
CA346760250
NM_001281493.2:c.2637C>A