Canonical Allele Identifier: PA2826633314
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410492
ClinVar RCV Id: RCV000464152 RCV000486385 RCV000491973 RCV004001845 RCV004539952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu885Gly
CA071386
NM_001281493.2:c.2654A>G