Canonical Allele Identifier: PA1139676947
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921115
ClinVar RCV Id: RCV001180265 RCV001875982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.[Ile1357delinsLeuVal;Glu1359delinsGlyGln]
CA1139656994
NM_000179.3:c.4016_4068dup