Canonical Allele Identifier: PA2826624685
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736886
ClinVar RCV Id: RCV002357802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys13Asn
CA346734529
NM_001281492.2:c.39G>C
CA346734530
NM_001281492.2:c.39G>T