Canonical Allele Identifier: PA2826631073
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834364
ClinVar RCV Id: RCV003758332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu369Met
CA346750682
NM_001281493.2:c.1105T>A