Canonical Allele Identifier: PA658680204
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483842
ClinVar RCV Id: RCV000570685 RCV001070096 RCV001844201 RCV004001062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg178Leu
CA346738710
NM_000179.3:c.533G>T