Canonical Allele Identifier: PA2826627274
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89279
ClinVar RCV Id: RCV000074744 RCV000115389 RCV000212665 RCV000148650 RCV000409574 RCV000656572 RCV000524141 RCV000680176 RCV001353412 RCV001798252
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val670Leu
CA010185
NM_001281492.2:c.2008G>C