Canonical Allele Identifier: PA2826625239
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823398
ClinVar RCV Id: RCV001019618 RCV001860952 RCV003467653 RCV003238829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr193Asn
CA346740929
NM_001281492.2:c.578C>A