Canonical Allele Identifier: PA2826635610
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410451
ClinVar RCV Id: RCV000470045 RCV000491796 RCV001565312 RCV004001833 RCV003463933
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro371Ala
CA068368
NM_001281494.2:c.1111C>G