Canonical Allele Identifier: PA658681300
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479892
ClinVar RCV Id: RCV000574714 RCV001204987 RCV001799687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1099Thr
CA346758472
NM_000179.3:c.3296T>C