Canonical Allele Identifier: PA2826625150
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630179
ClinVar RCV Id: RCV000775313 RCV000799448 RCV004001442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met173Thr
CA346740714
NM_001281492.2:c.518T>C