Canonical Allele Identifier: PA916012158
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141924
ClinVar RCV Id: RCV000130636 RCV000556805 RCV001030499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala928Gly
CA013825
NM_001281494.2:c.2783C>G