Canonical Allele Identifier: PA2826627557
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479929
ClinVar RCV Id: RCV000570721 RCV000588628 RCV000692110 RCV001821659 RCV003459291 RCV004000882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met738Ile
CA069280
NM_001281492.2:c.2214G>A
CA346754948
NM_001281492.2:c.2214G>C
CA346754949
NM_001281492.2:c.2214G>T