Canonical Allele Identifier: PA2826626863
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418326
ClinVar RCV Id: RCV000486361 RCV001355364 RCV001193732 RCV000563641 RCV000703273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met573Thr
CA16617666
NM_001281492.2:c.1718T>C