Canonical Allele Identifier: PA2826629158
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824364
ClinVar RCV Id: RCV001021401 RCV001046834 RCV003478645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1171Asp
CA346761421
NM_001281492.2:c.3511A>G