Canonical Allele Identifier: PA2742001594
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2920836
ClinVar RCV Id: RCV003736403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Val1525Met
CA354227043
NM_053027.4:c.4573G>A