Canonical Allele Identifier: PA1139674363
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921905
ClinVar RCV Id: RCV001181659 RCV001876033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu647Gln
CA346750456
NM_000179.3:c.1940T>A