Canonical Allele Identifier: PA2826628984
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719480
ClinVar RCV Id: RCV002303753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1141Leu
CA072180
NM_001281492.2:c.3421G>C
CA346761229
NM_001281492.2:c.3421G>T