Canonical Allele Identifier: PA645384648
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_000170.1:p.Glu1254_Asp1255delinsAspTyr
CA10582089
NM_000179.3:c.3762_3763delinsTT