Canonical Allele Identifier: PA1139674847
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935359
ClinVar RCV Id: RCV001203930 RCV002307698 RCV004010633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val762Ile
CA346752910
NM_000179.3:c.2284G>A