Canonical Allele Identifier: PA2826630805
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489972
ClinVar RCV Id: RCV000580753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser309Asn
CA346749553
NM_001281493.2:c.926G>A