Canonical Allele Identifier: PA2830142620
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2098431
ClinVar RCV Id: RCV003030946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444256.3:p.Asn1436Ser
CA071787
NM_053028.4:c.4307A>G