Canonical Allele Identifier: PA658680794
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 449885
ClinVar RCV Id: RCV000523105 RCV000579875 RCV000629977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser664Leu
CA346750650
NM_000179.3:c.1991C>T