Canonical Allele Identifier: PA160918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127593
ClinVar RCV Id: RCV000115423 RCV000121588 RCV000656903 RCV000662548 RCV000764435 RCV001079217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1263His
CA014284
NM_000179.3:c.3788G>A