Canonical Allele Identifier: PA2826633535
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455278
ClinVar RCV Id: RCV000550158 RCV002350168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu932Lys
CA46719352
NM_001281493.2:c.2794_2796delinsAAG
CA346760977
NM_001281493.2:c.2794G>A