Canonical Allele Identifier: PA2826631603
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135835
ClinVar RCV Id: RCV000160681 RCV000172814 RCV000412250 RCV000588994 RCV001084037 RCV003149835 RCV003493450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile493Thr
CA010164
NM_001281493.2:c.1478T>C