Canonical Allele Identifier: PA2830030500
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000306047
ClinVar Variation:
329931
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Gln1157Leu
CA9593262
NM_024729.4:c.3470A>T