Canonical Allele Identifier: PA2826627155
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237155
ClinVar RCV Id: RCV000234432 RCV000418671 RCV000758668 RCV001015160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg642Gln
CA068814
NM_001281492.2:c.1925G>A