Canonical Allele Identifier: PA645383567
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410436
ClinVar RCV Id: RCV000623149 RCV000491375 RCV002051855 RCV002230108 RCV002272245 RCV004001829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1063Arg
CA16610953
NM_000179.3:c.3188T>G