Canonical Allele Identifier: PA2826637629
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731849
ClinVar RCV Id: RCV002337523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro859Ser
CA346760134
NM_001281494.2:c.2575C>T