Canonical Allele Identifier: PA1139753394
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 936761
ClinVar RCV Id: RCV001205625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Val730Leu
CA354234081
NM_053027.4:c.2188G>T
CA354234082
NM_053027.4:c.2188G>C