Canonical Allele Identifier: PA1139676546
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845670
ClinVar RCV Id: RCV001048782 RCV002374893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1318Gly
CA346761525
NM_000179.3:c.3952A>G