Canonical Allele Identifier: PA2826633593
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332649
ClinVar RCV Id: RCV001805695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser944_Thr945insIlePheSer
CA2573051972
NM_001281493.2:c.2825_2833dup