Canonical Allele Identifier: PA2826629612
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768455
ClinVar RCV Id: RCV002387363 RCV003759658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile27Thr
CA346741074
NM_001281493.2:c.80T>C