Canonical Allele Identifier: PA916012178
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525686
ClinVar RCV Id: RCV000629876 RCV004002778 RCV002343196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile937Val
CA346761006
NM_001281494.2:c.2809A>G