Canonical Allele Identifier: PA2826627340
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525761
ClinVar RCV Id: RCV000630035 RCV002457989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro686Ala
CA346754059
NM_001281492.2:c.2056C>G