Canonical Allele Identifier: PA645382136
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234499
ClinVar RCV Id: RCV000220482 RCV002450643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu812Ile
CA10577275
NM_000179.3:c.2434C>A