Canonical Allele Identifier: PA2826632003
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477364
ClinVar RCV Id: RCV001971558 RCV002256878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val588Asp
CA346755239
NM_001281493.2:c.1763T>A