Canonical Allele Identifier: PA2826631092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89239
ClinVar RCV Id: RCV000219265 RCV000541319 RCV000662844 RCV003460667 RCV003151745
ClinVar Variation Id: 1784644
ClinVar RCV Id: RCV002419673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu373Asp
CA009565
NM_001281493.2:c.1119G>C
CA346750709
NM_001281493.2:c.1119G>T