Canonical Allele Identifier: PA192035
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185467
ClinVar RCV Id: RCV000164895 RCV000663227 RCV001037948 RCV002281982 RCV002255308 RCV003995375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His578Tyr
CA009101
NM_000179.3:c.1732C>T