Canonical Allele Identifier: PA2826636155
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435940
ClinVar RCV Id: RCV002001963
ClinVar Variation Id: 2587349
ClinVar RCV Id: RCV003360824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val499Leu
CA346753924
NM_001281494.2:c.1495G>T
CA346753925
NM_001281494.2:c.1495G>C