Canonical Allele Identifier: PA2826627102
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 640341
ClinVar RCV Id: RCV001190571 RCV000793348 RCV001193700 RCV001257482 RCV003314645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg631Thr
CA068739
NM_001281492.2:c.1892G>C