Canonical Allele Identifier: PA916012074
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 651578
ClinVar RCV Id: RCV000806972 RCV002336645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile898Thr
CA346760550
NM_001281494.2:c.2693T>C