Canonical Allele Identifier: PA2826633301
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser883Ala
CA013340
NM_001281493.2:c.2647T>G