Canonical Allele Identifier: PA658801972
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525820
ClinVar RCV Id: RCV000630150 RCV000771540 RCV004002793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp284His
CA346740545
NM_000179.3:c.850G>C