Canonical Allele Identifier: PA2826630157
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142264
ClinVar RCV Id: RCV000131285 RCV000479474 RCV000548616 RCV002509239 RCV003998097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser157Cys
CA008555
NM_001281493.2:c.470C>G