Canonical Allele Identifier: PA2825088066
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769757
ClinVar RCV Id: RCV002385540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met438Ile
CA346744388
NM_000179.3:c.1314G>A
CA346744389
NM_000179.3:c.1314G>C
CA346744390
NM_000179.3:c.1314G>T