Canonical Allele Identifier: PA915964582
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 649497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu638Ile
CA346750198
NM_000179.3:c.1912C>A