Canonical Allele Identifier: PA2826627430
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127572
ClinVar RCV Id: RCV000115392 RCV000195931 RCV000212667 RCV000412127 RCV001193702 RCV001354925 RCV003460814 RCV003997241
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His707Gln
CA010333
NM_001281492.2:c.2121C>G
CA346754300
NM_001281492.2:c.2121C>A