Canonical Allele Identifier: PA2826635990
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789060
ClinVar RCV Id: RCV002446208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp461Glu
CA346752948
NM_001281494.2:c.1383T>A
CA346752954
NM_001281494.2:c.1383T>G