Canonical Allele Identifier: PA167815
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142232
ClinVar RCV Id: RCV000131231 RCV000764426 RCV001060704 RCV001290553 RCV003998092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1005Gln
CA011349
NM_000179.3:c.3014G>A