Canonical Allele Identifier: PA2826634253
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823256
ClinVar RCV Id: RCV001019361 RCV001054837 RCV003461379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser13Pro
CA346740783
NM_001281494.2:c.37T>C