Canonical Allele Identifier: PA658680348
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455355
ClinVar RCV Id: RCV000550227 RCV002376987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val294Asp
CA346740670
NM_000179.3:c.881T>A