Canonical Allele Identifier: PA2826587494
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747524
ClinVar RCV Id: RCV003593638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys1035Trp
CA346761639
NM_001281494.2:c.3105C>G