Canonical Allele Identifier: PA2826634127
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_001268422.1:p.Val1043_Ala1045del
CA348238
NM_001281493.2:c.3128_3136del