Canonical Allele Identifier: PA2825119176
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026821
ClinVar RCV Id: RCV001327322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Ile210Phe
CA374115066
NM_000264.5:c.628A>T