Canonical Allele Identifier: PA916051279
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 808623
ClinVar RCV Id: RCV000996976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Arg98His
CA309565626
NM_024729.4:c.293G>A