Canonical Allele Identifier: PA2826587453
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89506
ClinVar RCV Id: RCV000074974 RCV000160701 RCV000202090 RCV000491705 RCV000542786 RCV000576708 RCV001355904
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg1032Gln
CA015202
NM_001281494.2:c.3095G>A