Canonical Allele Identifier: PA169089
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142674
ClinVar RCV Id: RCV000132027 RCV002228668 RCV003231160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro590Leu
CA009151
NM_000179.3:c.1769C>T