Canonical Allele Identifier: PA2826628899
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127591
ClinVar RCV Id: RCV000115421 RCV000196523 RCV000212688 RCV000656901 RCV001355140 RCV003467041 RCV001139791 RCV003997251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1123Glu
CA014183
NM_001281492.2:c.3368T>A