Canonical Allele Identifier: PA916011033
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419118
ClinVar RCV Id: RCV000487030 RCV000538832 RCV000776541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro57Leu
CA16617618
NM_001281492.2:c.170C>T