Canonical Allele Identifier: PA1139672599
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928046
ClinVar RCV Id: RCV001211347 RCV001191696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly289Arg
CA346740612
NM_000179.3:c.865G>C