Canonical Allele Identifier: PA133521
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 44081
ClinVar RCV Id: RCV000037057 RCV000295670 RCV002054632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Pro31Thr
CA133520
NM_001145809.2:c.91C>A