Canonical Allele Identifier: PA2825088767
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074426
ClinVar RCV Id: RCV004013960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys603Asn
CA346749377
NM_000179.3:c.1809G>C
CA346749378
NM_000179.3:c.1809G>T