Canonical Allele Identifier: PA2826628705
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 221107
ClinVar RCV Id: RCV000204393 RCV000662541 RCV000781594 RCV001020770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1082Met
CA348626
NM_001281492.2:c.3244G>A