Canonical Allele Identifier: PA2826626573
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479958
ClinVar RCV Id: RCV000564992 RCV003451218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu507Pro
CA346750185
NM_001281492.2:c.1520T>C