Canonical Allele Identifier: PA2825086624
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2431623
ClinVar RCV Id: RCV003142259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu228Val
CA346739896
NM_000179.3:c.683A>T