Canonical Allele Identifier: PA2826630719
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568393
ClinVar RCV Id: RCV000688742 RCV002397381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro289Gln
CA346749161
NM_001281493.2:c.866C>A