Canonical Allele Identifier: PA2826631467
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234795
ClinVar RCV Id: RCV000220828 RCV002450651 RCV002267973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr462Ile
CA10577273
NM_001281493.2:c.1385C>T