Canonical Allele Identifier: PA2826633351
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525810
ClinVar RCV Id: RCV000630131 RCV002457990 RCV004002792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser893Thr
CA071428
NM_001281493.2:c.2678G>C