Canonical Allele Identifier: PA645438704
Gene: MYL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 409234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000423.2:p.Pro144Thr
CA042991
NM_000432.4:c.430C>A