Canonical Allele Identifier: PA2826633223
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720068
ClinVar RCV Id: RCV002305085 RCV003308118
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro867Arg
CA346760181
NM_001281493.2:c.2600C>G