Canonical Allele Identifier: PA658746421
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495708
ClinVar RCV Id: RCV000586211 RCV001178184
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr786Asn
CA346753566
NM_000179.3:c.2356T>A