Canonical Allele Identifier: PA916011018
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455145
ClinVar RCV Id: RCV000526938 RCV002404365 RCV003222015 RCV004003664
ClinVar Variation Id: 1774384
ClinVar RCV Id: RCV002392386 RCV003095282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser51Arg
CA067823
NM_001281492.2:c.153C>G
CA346734939
NM_001281492.2:c.151A>C
CA346734945
NM_001281492.2:c.153C>A