Canonical Allele Identifier: PA2826630019
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89183
ClinVar RCV Id: RCV000570856 RCV001063935 RCV003466932 RCV003997064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile123Val
CA008413
NM_001281493.2:c.367A>G