Canonical Allele Identifier: PA2826636636
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410385
ClinVar RCV Id: RCV000759140 RCV002230099
ClinVar Variation Id: 801221
ClinVar RCV Id: RCV000985835 RCV002549655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Trp610Arg
CA16610945
NM_001281494.2:c.1828T>C
CA346755380
NM_001281494.2:c.1828T>A