Canonical Allele Identifier: PA916010918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184992
ClinVar RCV Id: RCV000164343 RCV000793874 RCV001795287 RCV003462130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro15Ser
CA015522
NM_001281492.2:c.43C>T