Canonical Allele Identifier: PA2826637715
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076149
ClinVar RCV Id: RCV004018466
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala904Thr
CA346760578
NM_001281494.2:c.2710G>A