Canonical Allele Identifier: PA2826636132
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455195
ClinVar RCV Id: RCV000558096 RCV001015335 RCV001811026 RCV004003678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile493Val
CA46711010
NM_001281494.2:c.1477A>G