Canonical Allele Identifier: PA645380329
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val509Leu
CA10578073
NM_000179.3:c.1525G>C
CA346746442
NM_000179.3:c.1525G>T