Canonical Allele Identifier: PA913192137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619578
ClinVar RCV Id: RCV000758670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu887Pro
CA346755201
NM_000179.3:c.2660T>C