Canonical Allele Identifier: PA132167
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 43121
ClinVar RCV Id: RCV000157371 RCV000158937 RCV000238674 RCV000618276 RCV000538349 RCV000755682 RCV003318341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Ala57Asp
CA013575
NM_000258.3:c.170C>A