Canonical Allele Identifier: PA2826631382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788141
ClinVar RCV Id: RCV002428269 RCV003101150
ClinVar Variation Id: 1788142
ClinVar RCV Id: RCV002420145 RCV003101151 RCV004007410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu442Asp
CA346752518
NM_001281493.2:c.1326G>C
CA346752527
NM_001281493.2:c.1326G>T