Canonical Allele Identifier: PA2830137498
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2920836
ClinVar RCV Id: RCV003736403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444253.3:p.Val1525Met
CA354227043
NM_053025.4:c.4573G>A