Canonical Allele Identifier: PA189907
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89368
ClinVar RCV Id: RCV000164048 RCV000433110 RCV000412287 RCV000524168 RCV000985842 RCV003997087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1095His
CA012443
NM_000179.3:c.3284G>A