Canonical Allele Identifier: PA645385144
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 252468
ClinVar RCV Id: RCV000239122 RCV001021599 RCV001046197 RCV003463708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1331Leu
CA072455
NM_000179.3:c.3992G>T