Canonical Allele Identifier: PA658680849
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455178
ClinVar RCV Id: RCV000550483 RCV000572538 RCV001548306 RCV004003671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr716Ala
CA068496
NM_000179.3:c.2146A>G