Canonical Allele Identifier: PA338883
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216297
ClinVar RCV Id: RCV001011654 RCV001340457 RCV003996994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu484Lys
CA338881
NM_000179.3:c.1450G>A