Canonical Allele Identifier: PA2825092298
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 937266
ClinVar RCV Id: RCV001206239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1263_Gly1265del
CA1139656978
NM_000179.3:c.3788_3796del