Canonical Allele Identifier: PA2826630742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780101
ClinVar RCV Id: RCV002404160 RCV003100840
ClinVar Variation Id: 1780131
ClinVar RCV Id: RCV002407740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe294Leu
CA346749264
NM_001281493.2:c.880T>C
CA346749275
NM_001281493.2:c.882T>A
CA346749276
NM_001281493.2:c.882T>G