Canonical Allele Identifier: PA1139675533
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 962997
ClinVar RCV Id: RCV001236954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp857Ala
CA346754730
NM_000179.3:c.2570A>C