Canonical Allele Identifier: PA2826634105
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2609821
ClinVar RCV Id: RCV003376041 RCV003759830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser1038Ile
CA346761655
NM_001281493.2:c.3113G>T