Canonical Allele Identifier: PA916012060
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490006
ClinVar RCV Id: RCV000580875 RCV001860048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr895Asn
CA346760535
NM_001281494.2:c.2684C>A