Canonical Allele Identifier: PA2826628780
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1099Ser
CA013811
NM_001281492.2:c.3296A>G