Canonical Allele Identifier: PA2826629550
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1983475
ClinVar RCV Id: RCV002770293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg14Ser
CA346740809
NM_001281493.2:c.42G>C
CA346740811
NM_001281493.2:c.42G>T