Canonical Allele Identifier: PA2826629547
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479920
ClinVar RCV Id: RCV000566795 RCV000586030 RCV000696871 RCV004000879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser13Cys
CA073607
NM_001281493.2:c.38C>G