Canonical Allele Identifier: PA2826626692
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 578579
ClinVar RCV Id: RCV000701633 RCV002422572 RCV003315441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser534Ala
CA346750647
NM_001281492.2:c.1600T>G