Canonical Allele Identifier: PA2499229375
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro320Thr
CA073647
NM_000179.3:c.958C>A