Canonical Allele Identifier: PA2826629271
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428408
ClinVar RCV Id: RCV000491543 RCV001856944 RCV004003464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1192Val
CA072394
NM_001281492.2:c.3575A>T