Canonical Allele Identifier: PA2826633934
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736284
ClinVar RCV Id: RCV002357563
ClinVar Variation Id: 2819276
ClinVar RCV Id: RCV003760967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu1009Asp
CA072317
NM_001281493.2:c.3027A>C
CA346761486
NM_001281493.2:c.3027A>T