Canonical Allele Identifier: PA2826637326
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410490
ClinVar RCV Id: RCV000462862 RCV000775731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met772Thr
CA16611034
NM_001281494.2:c.2315T>C