Canonical Allele Identifier: PA2826625022
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237215
ClinVar RCV Id: RCV000232347 RCV000561246 RCV000582421 RCV003233509 RCV003463644 RCV003998733 RCV003491994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly143Val
CA073459
NM_001281492.2:c.428G>T