Canonical Allele Identifier: PA2826624928
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89565
ClinVar RCV Id: RCV000506023 RCV000803732 RCV001026537 RCV003997103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile121Met
CA016429
NM_001281492.2:c.363A>G