Canonical Allele Identifier: PA645382996
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234533
ClinVar RCV Id: RCV000214691 RCV000461768 RCV000573070 RCV000657064 RCV003153515 RCV003998622
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile967Val
CA10577283
NM_000179.3:c.2899A>G