Canonical Allele Identifier: PA2826632069
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 942331
ClinVar RCV Id: RCV001212305 RCV003363169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp602Asn
CA346755337
NM_001281493.2:c.1804G>A