Canonical Allele Identifier: PA2826632280
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229879
ClinVar RCV Id: RCV000213285 RCV000485366 RCV000555735 RCV000781579 RCV001355880 RCV003335237 RCV003462414 RCV003997779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu651Lys
CA069715
NM_001281493.2:c.1951G>A