Canonical Allele Identifier: PA645382015
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433914
ClinVar RCV Id: RCV000589271 RCV000664307 RCV002527180 RCV004023356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro781Leu
CA346753452
NM_000179.3:c.2342C>T