Canonical Allele Identifier: PA2826635963
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000788
ClinVar RCV Id: RCV001296962 RCV002447270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr455Ile
CA346752828
NM_001281494.2:c.1364C>T