Canonical Allele Identifier: PA2826629461
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_001268421.1:p.[Ile1227delinsLeuVal;Glu1229delinsGlyGln]
CA1139656994
NM_001281492.2:c.3626_3678dup