Canonical Allele Identifier: PA2826625798
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676816
ClinVar RCV Id: RCV003461948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Trp326Cys
CA346744884
NM_001281492.2:c.978G>C
CA346744888
NM_001281492.2:c.978G>T