Canonical Allele Identifier: PA2826629920
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1747728
ClinVar RCV Id: RCV002349780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp99Tyr
CA346743420
NM_001281493.2:c.295G>T