Canonical Allele Identifier: PA2826629059
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142738
ClinVar RCV Id: RCV000132112 RCV000168184 RCV000708894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile1153Val
CA014555
NM_001281492.2:c.3457A>G