Canonical Allele Identifier: PA2573097951
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1317223
ClinVar RCV Id: RCV001759095 RCV002477999 RCV002334684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Lys1531Asn
CA071839
NM_053027.4:c.4593G>C
CA354226994
NM_053027.4:c.4593G>T