Canonical Allele Identifier: PA2826633473
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428303
ClinVar RCV Id: RCV000491642 RCV002268131 RCV001370230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe920Val
CA071813
NM_001281493.2:c.2758T>G