Canonical Allele Identifier: PA2830397362
Gene: MYL9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2241405
ClinVar RCV Id: RCV004103364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852667.1:p.Lys116Asn
CA408799076
NM_181526.3:c.348A>C
CA408799079
NM_181526.3:c.348A>T