Canonical Allele Identifier: PA2826636587
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224582
ClinVar RCV Id: RCV000210111 RCV000217860 RCV000693978 RCV002469072
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg599Ser
CA069480
NM_001281494.2:c.1795C>A