Canonical Allele Identifier: PA2826636201
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821272
ClinVar RCV Id: RCV001015525 RCV002549421
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu510Pro
CA346754038
NM_001281494.2:c.1529T>C