Canonical Allele Identifier: PA2825089539
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790082
ClinVar RCV Id: RCV002448480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr786Asp
CA346753575
NM_000179.3:c.2356T>G