Canonical Allele Identifier: PA2826628600
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231639
ClinVar RCV Id: RCV000218856 RCV000482279 RCV000558107 RCV001798716 RCV003462471 RCV003493521 RCV003997917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1059Ala
CA071392
NM_001281492.2:c.3175A>G