Canonical Allele Identifier: PA2830137501
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1317223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444253.3:p.Lys1531Asn
CA071839
NM_053025.4:c.4593G>C
CA354226994
NM_053025.4:c.4593G>T