Canonical Allele Identifier: PA2826625978
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232251
ClinVar RCV Id: RCV000223633 RCV000467079 RCV001093674 RCV001354875 RCV004532793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His371Tyr
CA067771
NM_001281492.2:c.1111C>T