Canonical Allele Identifier: PA2826630358
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val207Leu
CA10578073
NM_001281493.2:c.619G>C
CA346746442
NM_001281493.2:c.619G>T