Canonical Allele Identifier: PA2742001587
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2912060
ClinVar RCV Id: RCV003642234 RCV004374280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Ser1499Thr
CA354227224
NM_053027.4:c.4495T>A