Canonical Allele Identifier: PA2826625112
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419786
ClinVar RCV Id: RCV000486950 RCV000814413 RCV002446923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys165Glu
CA16617639
NM_001281492.2:c.493A>G