Canonical Allele Identifier: PA916010913
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233451
ClinVar RCV Id: RCV000214023 RCV001058725 RCV003462525 RCV003221870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser14Ala
CA10578020
NM_001281492.2:c.40T>G