Canonical Allele Identifier: PA658680485
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455119
ClinVar RCV Id: RCV000529516 RCV001010152 RCV003320670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala393Gly
CA067262
NM_000179.3:c.1178C>G