Canonical Allele Identifier: PA2826635982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 640341
ClinVar RCV Id: RCV001190571 RCV000793348 RCV001193700 RCV001257482 RCV003314645
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg459Thr
CA068739
NM_001281494.2:c.1376G>C