Canonical Allele Identifier: PA294418
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142496
ClinVar RCV Id: RCV000131641 RCV000204601 RCV000212656 RCV000410949 RCV001354229 RCV003462017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys676Arg
CA009570
NM_000179.3:c.2027A>G