Canonical Allele Identifier: PA2826636130
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 580724
ClinVar RCV Id: RCV000704351 RCV003153819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile493Met
CA346753787
NM_001281494.2:c.1479A>G