Canonical Allele Identifier: PA2826635586
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_001268423.1:p.Asp365Asn
CA346750661
NM_001281494.2:c.1093G>A