Canonical Allele Identifier: PA2826634293
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410445
ClinVar RCV Id: RCV000466844 RCV000579969 RCV004022782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr21Ile
CA073667
NM_001281494.2:c.62C>T