Canonical Allele Identifier: PA357376
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220192
ClinVar RCV Id: RCV000204219 RCV000216919 RCV000588780 RCV003997621
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr216Ile
CA073299
NM_000179.3:c.647C>T