Canonical Allele Identifier: PA645435131
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 44081
ClinVar RCV Id: RCV000037057 RCV000295670 RCV002054632
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Pro31Thr
CA133520
NM_024729.4:c.91C>A