Canonical Allele Identifier: PA2826631527
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89270
ClinVar RCV Id: RCV000130193 RCV003997074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Trp475Arg
CA010044
NM_001281493.2:c.1423T>A
CA346753332
NM_001281493.2:c.1423T>C