Canonical Allele Identifier: PA2826637029
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_001268423.1:p.Arg703Gln
CA011349
NM_001281494.2:c.2108G>A