Canonical Allele Identifier: PA916010903
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185016
ClinVar RCV Id: RCV000164368 RCV000985840
ClinVar Variation Id: 628563
ClinVar RCV Id: RCV000773055 RCV002534049
ClinVar Variation Id: 1797436
ClinVar RCV Id: RCV002438061 RCV003594302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe10Leu
CA011525
NM_001281492.2:c.30C>G
CA069791
NM_001281492.2:c.28T>C
CA346734516
NM_001281492.2:c.30C>A