Canonical Allele Identifier: PA1139675332
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 993195
ClinVar RCV Id: RCV001284515 RCV001370089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys824Glu
CA346754121
NM_000179.3:c.2470A>G