Canonical Allele Identifier: PA2826635602
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834364
ClinVar RCV Id: RCV003758332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu369Met
CA346750682
NM_001281494.2:c.1105T>A