Canonical Allele Identifier: PA299511
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182657
ClinVar RCV Id: RCV000160712 RCV000499861 RCV000214500 RCV000818095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr327Ala
CA016717
NM_000179.3:c.979A>G