Canonical Allele Identifier: PA2829518522
Gene: ACVR1B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004293.1:p.Leu16Phe
CA384883685
NM_004302.5:c.46C>T