Canonical Allele Identifier: PA916012031
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89421
ClinVar RCV Id: RCV000478227 RCV000582224 RCV000685790 RCV003450973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser886Asn
CA013469
NM_001281494.2:c.2657G>A