Canonical Allele Identifier: PA2826629604
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921522
ClinVar RCV Id: RCV001180967 RCV001876011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser26Ile
CA346741057
NM_001281493.2:c.77G>T