Canonical Allele Identifier: PA2826631386
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410415
ClinVar RCV Id: RCV000473197 RCV000663137 RCV001014897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile443Met
CA068645
NM_001281493.2:c.1329T>G