Canonical Allele Identifier: PA916011019
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 631192
ClinVar RCV Id: RCV000777354 RCV001203220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser51Ile
CA346734944
NM_001281492.2:c.152G>T