Canonical Allele Identifier: PA645382161
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237157
ClinVar RCV Id: RCV000234046 RCV000564117 RCV003469133 RCV003998717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu815Ile
CA10582062
NM_000179.3:c.2443C>A