Canonical Allele Identifier: PA296996
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181447
ClinVar RCV Id: RCV000158960 RCV003532002
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Pro65Ser
CA013638
NM_000258.3:c.193C>T