Canonical Allele Identifier: PA2826628902
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134856
ClinVar RCV Id: RCV000121589 RCV000160698 RCV000206271 RCV000411602 RCV000656902 RCV003460856 RCV003997354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1123Ala
CA014193
NM_001281492.2:c.3368T>C