Canonical Allele Identifier: PA1139690936
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 956952
ClinVar RCV Id: RCV001229851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp911His
CA346760614
NM_001281494.2:c.2731G>C