Canonical Allele Identifier: PA916011548
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479897
ClinVar RCV Id: RCV000562018 RCV002526787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser7Tyr
CA073578
NM_001281494.2:c.20C>A