Canonical Allele Identifier: PA645384802
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231365
ClinVar RCV Id: RCV000216678 RCV000708893 RCV000704640 RCV001358640 RCV003469028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1281Gln
CA10578163
NM_000179.3:c.3841G>C