Canonical Allele Identifier: PA2826626382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831521
ClinVar RCV Id: RCV003758275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val464Asp
CA346749244
NM_001281492.2:c.1391T>A