Canonical Allele Identifier: PA916010912
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410465
ClinVar RCV Id: RCV000458284 RCV000679240 RCV000771457 RCV003463935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys13Arg
CA072266
NM_001281492.2:c.38A>G