Canonical Allele Identifier: PA2826634622
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770040
ClinVar RCV Id: RCV002385823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly141Arg
CA346744489
NM_001281494.2:c.421G>A
CA346744493
NM_001281494.2:c.421G>C