Canonical Allele Identifier: PA2826628993
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455293
ClinVar RCV Id: RCV000538478 RCV000774615 RCV002264952 RCV003153677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1143Lys
CA072193
NM_001281492.2:c.3429T>G
CA346761246
NM_001281492.2:c.3429T>A