Canonical Allele Identifier: PA645381481
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232785
ClinVar RCV Id: RCV000218126 RCV000232938 RCV000684784 RCV002478805
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu700Ile
CA10578092
NM_000179.3:c.2098C>A