Canonical Allele Identifier: PA2826629401
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220947
ClinVar RCV Id: RCV000573760 RCV000986754 RCV001201374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1215_Ala1217del
CA348238
NM_001281492.2:c.3644_3652del