Canonical Allele Identifier: PA2826633635
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237197
ClinVar RCV Id: RCV000232565 RCV000478739 RCV000564937 RCV001818564
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu952_Asp953delinsAspTyr
CA10582089
NM_001281493.2:c.2856_2857delinsTT