Canonical Allele Identifier: PA2826635271
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419291
ClinVar RCV Id: RCV000485150 RCV000533746 RCV002402387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe294Ser
CA16617659
NM_001281494.2:c.881T>C