Canonical Allele Identifier: PA2826636264
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791909
ClinVar RCV Id: RCV002455599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn525Ser
CA346754167
NM_001281494.2:c.1574A>G