Canonical Allele Identifier: PA2826632318
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479947
ClinVar RCV Id: RCV000561841 RCV000629885 RCV001374579 RCV001355686 RCV001764641 RCV004000884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile660Thr
CA069760
NM_001281493.2:c.1979T>C