Canonical Allele Identifier: PA2826631270
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 655827
ClinVar RCV Id: RCV000812085 RCV002424910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val415Phe
CA346751107
NM_001281493.2:c.1243G>T