Canonical Allele Identifier: PA2826627352
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 960202
ClinVar RCV Id: RCV001233681 RCV003294110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu689Gln
CA346754077
NM_001281492.2:c.2065G>C