Canonical Allele Identifier: PA101382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89267
ClinVar RCV Id: RCV000074732 RCV000162422 RCV000218399 RCV000524139 RCV001353694 RCV002467437 RCV003466943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg772Trp
CA010016
NM_000179.3:c.2314C>T