Canonical Allele Identifier: PA645381743
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233162
ClinVar RCV Id: RCV000222866 RCV001035321 RCV001192487 RCV003998034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu747Arg
CA10578100
NM_000179.3:c.2240T>G