Canonical Allele Identifier: PA2825089083
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075039
ClinVar RCV Id: RCV004015565
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp667Asn
CA346750661
NM_000179.3:c.1999G>A