Canonical Allele Identifier: PA2826626621
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234553
ClinVar RCV Id: RCV000216304 RCV000567024 RCV001071803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser518Ile
CA10577270
NM_001281492.2:c.1553G>T