Canonical Allele Identifier: PA2826632989
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234689
ClinVar RCV Id: RCV000221433 RCV000561440 RCV003998640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys815Tyr
CA10577287
NM_001281493.2:c.2444G>A