Canonical Allele Identifier: PA1139690771
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 861324
ClinVar RCV Id: RCV001067830 RCV002451292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe872Tyr
CA346760214
NM_001281494.2:c.2615T>A