Canonical Allele Identifier: PA2826628571
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 576416
ClinVar RCV Id: RCV000698906 RCV001020591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1054Thr
CA071193
NM_001281492.2:c.3161T>C