Canonical Allele Identifier: PA916011057
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410430
ClinVar RCV Id: RCV000459237 RCV000761153 RCV000572922 RCV003335336 RCV003463930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser63Cys
CA16610836
NM_001281492.2:c.188C>G