Canonical Allele Identifier: PA2826633278
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233132
ClinVar RCV Id: RCV000220063 RCV000808376 RCV003998031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp879Gly
CA10578149
NM_001281493.2:c.2636A>G