Canonical Allele Identifier: PA645378238
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428443
ClinVar RCV Id: RCV000491335 RCV001328326 RCV001057562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly45Ala
CA346734900
NM_000179.3:c.134G>C