Canonical Allele Identifier: PA2826626691
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 449885
ClinVar RCV Id: RCV000523105 RCV000579875 RCV000629977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser534Leu
CA346750650
NM_001281492.2:c.1601C>T