Canonical Allele Identifier: PA2826634952
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775540
ClinVar RCV Id: RCV002392620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser223Arg
CA346746803
NM_001281494.2:c.667A>C
CA346746821
NM_001281494.2:c.669T>A
CA346746822
NM_001281494.2:c.669T>G