Canonical Allele Identifier: PA2825088329
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774467
ClinVar RCV Id: RCV002392469
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val508Leu
CA346746400
NM_000179.3:c.1522G>C
CA346746401
NM_000179.3:c.1522G>T