Canonical Allele Identifier: PA2826626929
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 945630
ClinVar RCV Id: RCV001216312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser588Arg
CA346751114
NM_001281492.2:c.1762A>C
CA346751122
NM_001281492.2:c.1764C>A
CA346751123
NM_001281492.2:c.1764C>G