Canonical Allele Identifier: PA197190
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187266
ClinVar RCV Id: RCV000166983 RCV000210183 RCV000693641 RCV001778764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys295Ile
CA016595
NM_000179.3:c.884A>T