Canonical Allele Identifier: PA1139689191
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 941121
ClinVar RCV Id: RCV001210838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro15Thr
CA346734535
NM_001281492.2:c.43C>A
CA1139655573
NM_001281492.2:c.42_43delinsAA