Canonical Allele Identifier: PA2826628519
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182647
ClinVar RCV Id: RCV000160695 RCV000464912 RCV000573393 RCV003998503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1043Met
CA013259
NM_001281492.2:c.3127G>A