Canonical Allele Identifier: PA2826632119
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455217
ClinVar RCV Id: RCV000536613 RCV002289716 RCV002438282 RCV003478107 RCV004003682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr612Ile
CA346755398
NM_001281493.2:c.1835C>T