Canonical Allele Identifier: PA658680970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455196
ClinVar RCV Id: RCV000527339 RCV002456040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp803Tyr
CA346753957
NM_000179.3:c.2407G>T