Canonical Allele Identifier: PA2826627059
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2803672
ClinVar RCV Id: RCV003760709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn621His
CA346752660
NM_001281492.2:c.1861A>C