Canonical Allele Identifier: PA2826636192
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791169
ClinVar RCV Id: RCV002450458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu508Asp
CA346754028
NM_001281494.2:c.1524G>T
CA346754029
NM_001281494.2:c.1524G>C