Canonical Allele Identifier: PA2826627068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234218
ClinVar RCV Id: RCV000219984 RCV000473229 RCV000985831 RCV003463605 RCV003998608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser623Cys
CA10578102
NM_001281492.2:c.1868C>G