Canonical Allele Identifier: PA164346
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141058
ClinVar RCV Id: RCV000129397 RCV000410431 RCV000477388 RCV000501569 RCV000622945 RCV001353758 RCV001257543 RCV001251301
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr767Ile
CA009983
NM_000179.3:c.2300C>T