Canonical Allele Identifier: PA2826632211
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 584536
ClinVar RCV Id: RCV000708718 RCV003594021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp634His
CA346755605
NM_001281493.2:c.1900G>C