Canonical Allele Identifier: PA658802252
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525637
ClinVar RCV Id: RCV000629764 RCV002431851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val801Met
CA346753926
NM_000179.3:c.2401G>A