Canonical Allele Identifier: PA2826587485
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487610
ClinVar RCV Id: RCV002008697 RCV003303579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val1034Ile
CA072783
NM_001281494.2:c.3100G>A