Canonical Allele Identifier: PA2826627073
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059653
ClinVar RCV Id: RCV001368982 RCV003462935 RCV003493850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr624Ile
CA346752760
NM_001281492.2:c.1871C>T