Canonical Allele Identifier: PA2826625912
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772977
ClinVar RCV Id: RCV002394633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu354Asp
CA346745706
NM_001281492.2:c.1062A>C
CA346745710
NM_001281492.2:c.1062A>T