Canonical Allele Identifier: PA160895
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89289
ClinVar RCV Id: RCV000129191 RCV000148652 RCV000121574 RCV000986723 RCV000585210 RCV001083699 RCV000764424 RCV001093694 RCV001353909 RCV003149719 RCV004528270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys854Met
CA010423
NM_000179.3:c.2561A>T