Canonical Allele Identifier: PA299469
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182640
ClinVar RCV Id: RCV000160686 RCV000212674 RCV000411475 RCV000475900 RCV000766283 RCV003998499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1024Gln
CA011493
NM_000179.3:c.3071G>A