Canonical Allele Identifier: PA2826629385
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 925341
ClinVar RCV Id: RCV001187217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1211_Asp1216del
CA913188078
NM_001281492.2:c.3632_3649del