Canonical Allele Identifier: PA2826636090
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 641281
ClinVar RCV Id: RCV000794488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His483Asp
CA346753552
NM_001281494.2:c.1447C>G