Canonical Allele Identifier: PA2826630299
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410487
ClinVar RCV Id: RCV000776440 RCV002230121 RCV002508935 RCV003446065
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala192Ser
CA067740
NM_001281493.2:c.574G>T