Canonical Allele Identifier: PA2826636537
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234455
ClinVar RCV Id: RCV000215122 RCV000473265 RCV001016279 RCV003998617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile589Met
CA069419
NM_001281494.2:c.1767C>G