Canonical Allele Identifier: PA2826627735
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230538
ClinVar RCV Id: RCV004520689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu778Asp
CA346755363
NM_001281492.2:c.2334A>C
CA346755364
NM_001281492.2:c.2334A>T