Canonical Allele Identifier: PA916012389
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428390
ClinVar RCV Id: RCV000490965 RCV001327278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn999_Arg1002del
CA645369296
NM_001281494.2:c.2995_3006del