Canonical Allele Identifier: PA2826633380
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733115
ClinVar RCV Id: RCV002455228 RCV003594200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu899Arg
CA346760556
NM_001281493.2:c.2696T>G