Canonical Allele Identifier: PA2826629623
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768750
ClinVar RCV Id: RCV002382967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu30Asp
CA346741137
NM_001281493.2:c.90A>T
CA346741142
NM_001281493.2:c.90A>C