Canonical Allele Identifier: PA2826625026
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_001268421.1:p.Ser144Asn
CA016514
NM_001281492.2:c.431G>A