Canonical Allele Identifier: PA1139676814
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 925341
ClinVar RCV Id: RCV001187217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1341_Asp1346del
CA913188078
NM_000179.3:c.4022_4039del