Canonical Allele Identifier: PA2826631588
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185830
ClinVar RCV Id: RCV000165325 RCV000537745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg489Cys
CA010130
NM_001281493.2:c.1465C>T