Canonical Allele Identifier: PA2826634332
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410486
ClinVar RCV Id: RCV002230120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr31Ser
CA16610874
NM_001281494.2:c.92C>G
CA346741146
NM_001281494.2:c.91A>T