Canonical Allele Identifier: PA2826625280
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410486
ClinVar RCV Id: RCV002230120
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr203Ser
CA16610874
NM_001281492.2:c.608C>G
CA346741146
NM_001281492.2:c.607A>T