Canonical Allele Identifier: PA2826637828
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064041
ClinVar RCV Id: RCV002928707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His964Gln
CA346761191
NM_001281494.2:c.2892T>A
CA346761192
NM_001281494.2:c.2892T>G