Canonical Allele Identifier: PA2826626062
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89200
ClinVar RCV Id: RCV000214996 RCV000556355 RCV000219119 RCV001194395 RCV000662803 RCV003460663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln392Arg
CA008795
NM_001281492.2:c.1175A>G