Canonical Allele Identifier: PA2826633356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410511
ClinVar RCV Id: RCV000467878 RCV000587963 RCV000574327 RCV002496782 RCV003470469 RCV004001852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu894Gln
CA071434
NM_001281493.2:c.2680G>C