Canonical Allele Identifier: PA2826635979
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140836
ClinVar RCV Id: RCV000129031 RCV000195792 RCV000657020 RCV000662484 RCV001002443 RCV003460882 RCV003997472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg459Gly
CA009950
NM_001281494.2:c.1375A>G