Canonical Allele Identifier: PA916011385
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525860
ClinVar RCV Id: RCV000630210 RCV002448931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile949Val
CA346758064
NM_001281492.2:c.2845A>G