Canonical Allele Identifier: PA2830142378
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 409705
ClinVar RCV Id: RCV000469933 RCV003168815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Ser1113Phe
CA069769
NM_053028.4:c.3338C>T