Canonical Allele Identifier: PA334465
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188262
ClinVar RCV Id: RCV000168238 RCV000214013 RCV000484522 RCV000662602 RCV000780480 RCV003462260 RCV003491921 RCV003995615
ClinVar Variation Id: 2773666
ClinVar RCV Id: RCV003585639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1247Ser
CA014131
NM_000179.3:c.3740C>G
CA346761053
NM_000179.3:c.3739A>T