Canonical Allele Identifier: PA916052017
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 216969
ClinVar RCV Id: RCV000198643 RCV002315630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Asp717Tyr
CA068222
NM_053027.4:c.2149G>T