Canonical Allele Identifier: PA2826633371
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser897Asn
CA10578150
NM_001281493.2:c.2690G>A