Canonical Allele Identifier: PA2826627129
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 574200
ClinVar RCV Id: RCV000696068 RCV002256476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His636Tyr
CA346752995
NM_001281492.2:c.1906C>T