Canonical Allele Identifier: PA2826628703
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219294
ClinVar RCV Id: RCV000206750 RCV000215362 RCV000471873 RCV003454537 RCV003462359 RCV003477675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1081Pro
CA350757
NM_001281492.2:c.3242T>C