Canonical Allele Identifier: PA357520
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220633
ClinVar RCV Id: RCV001012760 RCV001360388 RCV003997648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile570Val
CA068049
NM_000179.3:c.1708A>G