Canonical Allele Identifier: PA2826626157
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 126891
ClinVar RCV Id: RCV000114750 RCV000129248 RCV003593911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser411Arg
CA008929
NM_001281492.2:c.1231A>C
CA346747078
NM_001281492.2:c.1233C>G
CA346747082
NM_001281492.2:c.1233C>A