Canonical Allele Identifier: PA916012125
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142155
ClinVar RCV Id: RCV000131017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr917Asn
CA013750
NM_001281494.2:c.2750C>A