Canonical Allele Identifier: PA916011171
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89572
ClinVar RCV Id: RCV000129540 RCV000235182 RCV000411287 RCV000524216 RCV000985852 RCV000761154 RCV001798258 RCV004537285 RCV003460705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly159Glu
CA016554
NM_001281492.2:c.476_477delinsAA