Canonical Allele Identifier: PA1139689215
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 944227
ClinVar RCV Id: RCV001214582 RCV002339560 RCV003478736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala16Glu
CA346734543
NM_001281492.2:c.47C>A