Canonical Allele Identifier: PA916012115
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 653382
ClinVar RCV Id: RCV000809152
ClinVar Variation Id: 940856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val910Leu
CA346760609
NM_001281494.2:c.2728G>C
CA346760610
NM_001281494.2:c.2728G>T