Canonical Allele Identifier: PA916011056
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220796
ClinVar RCV Id: RCV000206061 RCV000217423 RCV000656886 RCV000765679 RCV003462390 RCV004530239 RCV000491346 RCV000663184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser63Pro
CA068241
NM_001281492.2:c.187T>C
CA2838032166
NM_001281492.2:c.186_187delinsAC