Canonical Allele Identifier: PA915965154
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 645219
ClinVar RCV Id: RCV000799261 RCV002487680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr895Arg
CA069436
NM_000179.3:c.2684C>G