Canonical Allele Identifier: PA2826630990
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231915
ClinVar RCV Id: RCV000214027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val351Ala
CA10578089
NM_001281493.2:c.1052T>C