Canonical Allele Identifier: PA2826586431
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735193
ClinVar RCV Id: RCV002355274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu970Ala
CA346761238
NM_001281494.2:c.2909A>C