Canonical Allele Identifier: PA2826636111
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790251
ClinVar RCV Id: RCV002457748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp488Ala
CA346753669
NM_001281494.2:c.1463A>C