Canonical Allele Identifier: PA2826625129
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 505514
ClinVar RCV Id: RCV000603999 RCV002448845 RCV002529344 RCV004002483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys169Glu
CA346740692
NM_001281492.2:c.505A>G