Canonical Allele Identifier: PA2826625193
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 371790
ClinVar RCV Id: RCV000410264 RCV000576046 RCV001361344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser184Asn
CA073598
NM_001281492.2:c.551G>A