Canonical Allele Identifier: PA2826633229
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630085
ClinVar RCV Id: RCV000775011 RCV003228987 RCV001069894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile868Val
CA346760184
NM_001281493.2:c.2602A>G