Canonical Allele Identifier: PA287348
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127606
ClinVar RCV Id: RCV000115444 RCV000222274 RCV000554997 RCV003997257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser274Asn
CA016514
NM_000179.3:c.821G>A