Canonical Allele Identifier: PA645381353
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 422162
ClinVar RCV Id: RCV000480051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly674Val
CA16617664
NM_000179.3:c.2021G>T