Canonical Allele Identifier: PA2826587450
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184389
ClinVar RCV Id: RCV000163638 RCV000198598 RCV000409323 RCV000657088 RCV001706075 RCV003462121 RCV003995266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg1032Trp
CA015093
NM_001281494.2:c.3094C>T