Canonical Allele Identifier: PA2826626635
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483822
ClinVar RCV Id: RCV000561961 RCV001240700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly522Arg
CA346750564
NM_001281492.2:c.1564G>C
CA346750569
NM_001281492.2:c.1564G>A