Canonical Allele Identifier: PA2826631639
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479914
ClinVar RCV Id: RCV000564287 RCV000985832 RCV000815080 RCV004000878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile503Val
CA46711082
NM_001281493.2:c.1507A>G