Canonical Allele Identifier: PA916012072
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220745
ClinVar RCV Id: RCV000204738 RCV000566750 RCV000791410 RCV002277568 RCV002243889 RCV003462389
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile898Val
CA071451
NM_001281494.2:c.2692A>G