Canonical Allele Identifier: PA2826631113
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523593
ClinVar RCV Id: RCV002038994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu377Trp
CA346750734
NM_001281493.2:c.1130T>G