Canonical Allele Identifier: PA658802539
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_000170.1:p.Ile1239Val
CA346761006
NM_000179.3:c.3715A>G